Company: Apitoria Pharma (A 100% subsidiary of Aurobindo Pharma)
Experience: 2 to 15 years Location: Hyderabad (Visakhapatnam Cluster, API Division) Qualification: M.Tech / B.Tech / M.Sc / B.Sc Position: Staff, Executive, Assistant Manager (AM), Deputy Manager (DM), Manager
About Aurobindo Pharma
Aurobindo Pharma is a global leader in the pharmaceutical industry. Apitoria Pharma, a 100% subsidiary, is hiring talented professionals for its Environment, Health & Safety (EHS) department. This is an exciting opportunity to be part of the Visakhapatnam Cluster in the API Division, located in Hyderabad. Aurobindo Pharma Hiring for EHS
Current Vacancies
Positions available for professionals with experience in EHS:
Staff
Executive
Assistant Manager (AM)
Deputy Manager (DM)
Manager
Role Details
Stream: Environmental, Process & General Safety
Key Responsibilities:
Expertise in work permits and general safety
Conducting mock drills and risk assessments
Managing ETP operations and waste management
Supervising firefighting systems and conducting training programs
Performing safety audits and ensuring compliance with statutory regulations
Medtronic, a global leader in medical technology, is offering a unique internship opportunity in Hyderabad for fresh graduates. This internship is an entry-level role designed to develop skills in MDR (Medical Device Reporting) Vigilance—a critical area within the medical device industry focused on monitoring product safety and ensuring compliance with regulatory standards. This role presents an excellent learning environment, ideal for recent graduates in pharmacy, life sciences, biotechnology, and related fields who are eager to jump-start their careers. Medtronic Internship MDR Vigilance Specialist
About Medtronic
Medtronic has a long-standing reputation as an innovative leader in the healthcare industry, pioneering advancements that improve patient care and make healthcare accessible worldwide. With a commitment to enhancing patient outcomes, Medtronic’s influence spans across therapeutic areas, and the company is known for nurturing its employees and fostering a work culture that emphasizes personal and professional growth. Medtronic’s focus on inclusivity and empowerment enables its employees to achieve impactful careers while making meaningful contributions to healthcare. Medtronic Internship MDR Vigilance Specialist
Role Overview: Intern – MDR Vigilance Specialist
As an Intern-MDR Vigilance Specialist, you will work within Medtronic’s vigilance and compliance team. MDR Vigilance involves monitoring, reporting, and addressing adverse events related to medical devices. This role is essential to ensuring patient safety and regulatory compliance, as well as improving the quality and reliability of Medtronic’s products. The internship offers a hands-on learning experience that will introduce you to medical device regulations, safety protocols, and the fundamentals of medical technology research. Medtronic Internship MDR Vigilance Specialist
Medtronic Internship MDR Vigilance Specialist
Key Responsibilities
In this role, you will be trained to assist in tasks that support Medtronic’s regulatory compliance and product safety goals. Key responsibilities include:
Technical Research Support: Assist in conducting research for service, product, or project groups within Medtronic. This research will often involve analyzing technical aspects of product design, safety data, and compliance requirements.
Project Assistance: Support the development, monitoring, and execution of technical projects. These projects may relate to new product launches, product improvements, or compliance initiatives, providing you with exposure to Medtronic’s structured project management processes.
Data Analysis and Reporting: Collect, analyze, and report data to help create clear and comprehensive internal reports. Your ability to provide accurate data will contribute to effective communication within the team and help with decision-making.
Workflow Familiarity: Develop a fundamental understanding of industry standards, regulatory requirements, and organizational workflows. Through this, you’ll gain insight into Medtronic’s approach to maintaining product safety and regulatory compliance.
Team Collaboration: Work closely with cross-functional team members to deliver on assigned tasks and develop essential project management skills. This collaboration will give you an understanding of teamwork in a high-impact corporate setting. Medtronic Internship MDR Vigilance Specialist
Differentiating Factors of the Internship
This internship will introduce you to the complexities of MDR Vigilance and compliance processes in a highly regulated industry, providing a valuable foundation in medical device safety. Key aspects that distinguish this role include:
Autonomy: Although you will work under close supervision, you’ll have opportunities to contribute meaningfully to projects, enhancing your decision-making skills as you grow more comfortable in the role.
Impact: Your work will have a measurable impact, even if limited to smaller projects or tasks. Through these contributions, you’ll gain an understanding of how even entry-level work supports broader organizational goals and improves patient outcomes.
Innovation and Complexity: Expect to engage in identifying and addressing minor challenges within existing processes. By doing so, you’ll not only develop problem-solving skills but also contribute to continuous process improvements.
Communication and Influence: While your interactions may be limited to your immediate team, this experience will help you learn the nuances of internal communication and collaboration within a large organization.
Leadership and Personal Growth: Medtronic values each employee’s growth. As an intern, you will receive mentorship to help you build essential skills, enhance your technical expertise, and grow into a well-rounded professional ready for more significant roles. Medtronic Internship MDR Vigilance Specialist
Medtronic Internship MDR Vigilance Specialist
Essential Qualifications and Skills
To succeed as an Intern-MDR Vigilance Specialist, candidates should meet the following requirements and exhibit key skills: Medtronic Internship MDR Vigilance Specialist
Educational Requirements: Candidates should possess a degree in fields relevant to the medical device and healthcare industries. Accepted qualifications include:
B.Pharm, M.Pharm, Pharm.D – Ideal for candidates with a background in pharmacy, as they’ll bring valuable knowledge of drug safety and pharmacology.
M.Sc, B.Sc, Life Sciences, Biotech – Ideal for candidates from scientific disciplines related to biology, biotechnology, and life sciences.
M.Tech – Suitable for candidates with a technical background, particularly in biotechnology or biomedical engineering.
Experience: This position is intended for fresh graduates with no prior professional experience, making it a perfect entry point for those looking to gain industry experience.
Key Skills:
Research and Analysis: Ability to assist in technical research and data analysis to support MDR Vigilance projects.
Coordination and Communication: Strong organizational skills to help manage project timelines, with a clear communication style that facilitates smooth team collaboration.
Problem-Solving: A proactive approach to problem-solving, focusing on minor changes that improve overall processes and workflows.
Adaptability and Willingness to Learn: Medtronic values interns who demonstrate an eagerness to learn and contribute, even if they’re new to the field. Medtronic Internship MDR Vigilance Specialist
Why Choose Medtronic?
Medtronic offers a nurturing, inclusive environment that prioritizes both professional and personal growth. Joining Medtronic as an intern provides:
Career Development: Gain hands-on experience with a global leader in medical technology, preparing you for future roles in MDR Vigilance, compliance, or other fields within healthcare.
Supportive Work Culture: Work in an environment that promotes collaboration, inclusivity, and continuous improvement, with experienced mentors to guide you along the way.
Global Impact: Contribute to a company that touches lives worldwide, enhancing the quality of life for patients by advancing healthcare through innovation. Medtronic Internship MDR Vigilance Specialist
Application Process
To apply for the Intern-MDR Vigilance Specialist position, submit your application online through Medtronic’s career portal. Be sure to attach a resume highlighting your educational background, relevant coursework, and any academic projects that may demonstrate your technical knowledge and problem-solving skills.
Final Tip: Emphasize your passion for healthcare, eagerness to learn, and willingness to contribute in a regulatory and compliance role. Medtronic seeks interns who are committed to making a difference.
The Intern-MDR Vigilance Specialist role at Medtronic is an exceptional opportunity for fresh graduates looking to enter the healthcare industry. With a focus on safety, compliance, and innovation, this internship will help you build foundational skills in MDR Vigilance while immersing you in Medtronic’s mission of enhancing patient care globally. For recent graduates in pharmacy, life sciences, biotechnology, or related fields, this internship provides a path to a rewarding career where you’ll make a difference in patients’ lives every day.
Zydus Lifesciences is inviting experienced professionals to join its team in Ahmedabad. We are seeking talent for multiple positions within Production, QA, QC, and IPQA departments, with a focus on drug substance manufacturing. This is a fantastic opportunity for individuals with a background in biotechnology who are looking to make a meaningful impact in the pharmaceutical and biotech industry. Production/ QA/ QC/ IPQA at Zydus Lifesciences
Job Highlights
Work-Life Balance
Flexibility
Time Management
Problem-Solving Skills
Walk-In Interview Details
Date: November 17, 2024 Time: 8:30 AM to 5:00 PM Venue: Hotel Radisson Blu, 136/1, Hinjewadi Phase 1 Rd, Behind Mahindra International School, Phase 1, Hinjawadi Rajiv Gandhi Infotech Park, Pune, Pimpri-Chinchwad, Maharashtra 411057 Contact Number: 020-69528000
Position Details
We are hiring for various roles in Production, Quality Assurance (QA), Quality Control (QC), and In-Process Quality Assurance (IPQA) at Zydus Biologics in Ahmedabad. Below is a detailed breakdown of the responsibilities and requirements for each area: Production/ QA/ QC/ IPQA at Zydus Lifesciences
Aurobindo Pharma Hiring for Trainee in Manufacturing API
Aurobindo Pharma (Lyfius Pharma) – Walk-In Interview for Trainee in Manufacturing API
Aurobindo Pharma Ltd’s subsidiary Lyfius Pharma is inviting freshers to join as Trainees in Manufacturing API at their Kakinada facility. This is an excellent opportunity for candidates with a background in Biotech, Biochemistry, or Chemical Engineering to start their careers in pharmaceutical biotechnology. Aurobindo Pharma Hiring for Trainee in Manufacturing API
Job Summary
Job Title
Trainee – Manufacturing API
Company
Lyfius Pharma (A subsidiary of Aurobindo Pharma Ltd)
Experience
Freshers
Location
Kakinada, Andhra Pradesh (A.V. Nagaram)
Qualification
B.Tech, M.Tech, M.Sc, or Diploma
Walk-in Date
November 10, 2024
Walk-in Time
9:00 AM onwards
Venue
Lyfius Pharma, A.V. Nagaram, Kakinada, AP
Aurobindo Pharma Hiring for Trainee in Manufacturing API
Position Details
Department: Manufacturing API
Role: Trainee
Location: Kakinada, Andhra Pradesh
Eligibility Criteria
Candidates must meet the following requirements:
Educational Qualification:
B.Tech in Biotech or Chemical Engineering
M.Tech in Biotech
M.Sc in Biotech/Biochemistry
Diploma in Chemical Engineering
Other Requirements:
No educational backlogs
Minimum of 60% marks in academics
Willingness to work in shifts, including night shifts
Aurobindo Pharma Hiring for Trainee in Manufacturing API
Job Responsibilities
As a Trainee in Manufacturing API, your responsibilities include:
Learning and Assisting: Engage in the API manufacturing process and collaborate with team members.
Maintaining Standards: Follow company guidelines and adhere to safety protocols.
Documentation: Prepare and maintain necessary records as part of the manufacturing process.
Operational Support: Ensure efficient functioning of the manufacturing processes. Aurobindo Pharma Hiring for Trainee in Manufacturing API
Why Join Lyfius Pharma?
Global Reach: Work for a subsidiary of Aurobindo Pharma, a globally recognized pharmaceutical leader.
Professional Growth: Gain hands-on experience in API manufacturing.
Collaborative Environment: Engage with a supportive team dedicated to innovation in biotechnology. Aurobindo Pharma Hiring for Trainee in Manufacturing API
How to Apply Scan the QR code with Google Lens for easy application. If you’re unable to attend, share this job with someone who might be interested.
Important Notice: Lyfius Pharma does not charge fees for job applications. Please beware of fraudulent offers and apply only through official channels. Aurobindo Pharma Hiring for Trainee in Manufacturing API
Career Opportunity at Aurigene Services: Scientist – Bioanalytical R&D
Aurigene Services, a leader in biologics Contract Development and Manufacturing (CDMO), is seeking a talented Scientist for their Bioanalytical R&D team in Hyderabad. This role is an excellent fit for professionals looking to enhance their expertise in bioanalytical research within an innovative and rapidly growing organization. Aurigene Services Hiring Scientist Bioanalytical R&D
About Aurigene Services
Aurigene Services specializes in providing high-quality CDMO solutions for biologics, offering support across the full spectrum of drug development. Known for its commitment to scientific excellence and customer-focused approach, Aurigene collaborates with global pharmaceutical and biotech companies to advance life-saving therapeutics. Joining Aurigene means becoming part of a pioneering team dedicated to innovation in biologics. Aurigene Services Hiring Scientist Bioanalytical R&D
Role Overview
As a Scientist in Bioanalytical R&D, you’ll perform hands-on bioanalytical work, including cell-based assays, ELISA, and ligand binding assays. Your contributions will directly impact the development of biologic drugs, making this a meaningful opportunity for those interested in applied science and data analysis. Aurigene Services Hiring Scientist Bioanalytical R&D
Business Unit: CDMO Biologics
Location: Hyderabad
Experience Required: 1 to 4 years
Qualifications: MSc / M.Tech in relevant scientific fields
Cell-Based Assays: Perform critical cell-based assays, ensuring accuracy and precision.
ELISA and Ligand Binding Assays: Conduct essential ligand binding assays, contributing valuable data for drug development.
2. Data Management and Analysis
Data Generation: Collect data from experiments and accurately record findings.
Report Writing: Prepare detailed analytical reports to document findings and support project decisions.
3. Technical Expertise
Additional Techniques: Knowledge in flow cytometry and Surface Plasmon Resonance (SPR) is highly valued.
Troubleshooting Skills: Resolve technical issues efficiently to maintain project timelines.
Ideal Candidate Profile
This position is suited for a professional with a strong foundation in bioanalytical techniques and a knack for data accuracy. Here’s what Aurigene is looking for:
Bioanalytical Skills: Proficiency in cell-based assays, ELISA, and ligand binding techniques.
Analytical Mindset: Ability to interpret data meticulously and ensure quality results.
Report Writing Abilities: Competent in compiling and presenting data findings effectively.
Attention to Detail: High standards for data integrity, essential for bioanalytical research.
Technical Proficiency: Familiarity with advanced techniques like flow cytometry and SPR adds value. Aurigene Services Hiring Scientist Bioanalytical R&D
Why Join Aurigene Services?
Aurigene offers a dynamic work environment focused on innovation and growth. Here are some key benefits of working at Aurigene:
Career Advancement: This role offers exposure to cutting-edge bioanalytical research and a pathway for career growth.
Learning Opportunities: Expand your expertise by working with advanced bioanalytical methods and collaborating with experts in the field.
Supportive Work Culture: Aurigene values work-life balance, flexibility, and fosters a collaborative culture.
Impactful Work: Contribute to drug development projects that make a difference in patients’ lives globally.
To apply, please send your updated resume to pranavgayal@aurigeneservices.com with the subject line “Scientist – Bioanalytical R&D”. Highlight your experience in bioanalytical techniques, data analysis, and any additional skills that make you a strong candidate for this role. Aurigene Services Hiring Scientist Bioanalytical R&D
This position with Aurigene Services offers a unique opportunity for scientists who are passionate about advancing their skills in bioanalytical research and contributing to the growth of innovative biologic therapies. Apply today to become a part of Aurigene’s forward-thinking team and make a real impact in healthcare!
Neuland U1, Veerabhadraswamy Temple Road, Jinnaram, Bonthapally Village, Telangana 502313
Contact
priyankapandey@neulandlabs.com
Neuland Hiring for Trainee / Chemist Production
Join Neuland Laboratories as a Production Trainee / Chemist
Neuland Laboratories Limited is offering a walk-in interview for a Trainee / Chemist – Production position, providing a promising start for recent graduates and entry-level candidates in pharmaceutical production. Neuland Laboratories, established in 1984, is a renowned API (Active Pharmaceutical Ingredients) manufacturer, known for its commitment to high standards in drug development and GMP (Good Manufacturing Practices) manufacturing. With an esteemed history and FDA-approved facilities, Neuland is a rewarding workplace for individuals looking to grow their careers in the pharmaceutical industry. Neuland Hiring for Trainee / Chemist Production
Role Overview
The Production Trainee / Chemist will be part of the production team responsible for maintaining seamless production operations within the manufacturing facility. This position ensures that batch processing is executed effectively and in line with Standard Operating Procedures (SOPs) and safety regulations, making it a vital role in the company’s operational workflow. Neuland Hiring for Trainee / Chemist Production
As a Trainee/Chemist, you’ll be involved in:
Batch Processing: Collecting and verifying batch manufacturing sheets from QA, ensuring each step adheres to process standards.
Process Operations: Executing manufacturing processes and updating real-time data in the Batch Manufacturing System (BMS).
Cleanliness & Calibration: Maintaining hygiene of equipment and monitoring calibration needs to keep production areas compliant.
Documentation: Accurately recording all production activities and collaborating with the QA department for thorough documentation.
Coordination & Maintenance: Reporting any deviations to production supervisors and coordinating with maintenance teams for regular equipment checks.
Neuland Hiring for Trainee / Chemist Production
Ideal Candidate Profile
Experience: This role is open to candidates with 0 to 4 years of experience in the Production Department of an API industry. This range makes it ideal for fresh graduates or individuals with early experience in the field.
Educational Qualifications: A background in Pharma is highly preferred. Accepted degrees include B.Pharm, M.Pharm, MSc, BSc, B.Tech, and M.Tech, ensuring applicants have the necessary scientific and technical foundation for the role. Neuland Hiring for Trainee / Chemist Production
Responsibilities and Key Tasks
1. Batch Manufacturing and Documentation
Receiving BMS Sheets: Collect batch manufacturing sheets from QA for each process and ensure all information is up-to-date.
Recording Process Data: Continuously monitor and document process parameters, helping ensure production runs smoothly.
Data Entry in BMS: Accurately update BMS with real-time data to reflect current operations and record any discrepancies. Neuland Hiring for Trainee / Chemist Production
2. Equipment Maintenance and Area Management
Hygiene Standards: Keep production areas clean, including process equipment, to maintain quality standards.
Observation & Calibration: Monitor equipment, report calibration needs, and ensure it’s ready for production. Neuland Hiring for Trainee / Chemist Production
3. Compliance and Safety
Deviation Reporting: Report any irregularities or equipment deviations to production officers.
Coordination with Maintenance: Work closely with maintenance teams for preventive equipment upkeep, which ensures production consistency.
4. Learning and Development
Participate in Training: Attend in-house training sessions to stay updated on the latest production techniques and safety protocols.
Neuland Hiring for Trainee / Chemist Production
Walk-In Interview Details
If you’re interested and meet the eligibility criteria, head to the Neuland Laboratories campus for a walk-in interview:
Fresher Candidates: Bring an updated resume and copies of your educational certificates. Graduates from 2022, 2023, and 2024 are eligible to apply for entry-level roles.
Experienced Candidates: Along with your resume, bring an increment letter and the last three months’ pay slips for verification.
If you have any questions regarding the position, you can contact Neuland Laboratories at priyankapandey@neulandlabs.com.
Why Work at Neuland?
Neuland Laboratories is an ideal workplace for candidates looking for growth and stability in the pharmaceutical industry. With a team of over 1,500 professionals and FDA-approved facilities, the company emphasizes excellence, quality, and innovation. As a Trainee or Chemist, you’ll gain hands-on experience and access to training programs that enhance your skills, all within a supportive work environment that values work/life balance, flexibility, and professional development. Neuland Hiring for Trainee / Chemist Production
Join Neuland and be part of a company that values expertise, quality, and a commitment to advancing the healthcare industry. Neuland Hiring for Trainee / Chemist Production
Position: Executive / Senior Executive – Quality Assurance Organization: Biological E. Limited Qualification: B.Pharmacy / M.Pharmacy / M.Sc. (Life Science) / M.Tech. (Life Science) Experience: 3 to 8 years Location: Hyderabad, Telangana Event: Walk-in Interview Date: Friday, October 25, 2024 Time: 09:00 AM – 02:30 PM
About Biological E. Limited
Biological E. Limited, committed to “Celebrating Life Every Day,” is a leader in vaccine production and pharmaceutical research. Located in Shamirpet, Hyderabad, BE is looking for talented, experienced, and self-motivated individuals to join their Quality Assurance team. If you have 3 to 8 years of experience in QA and are passionate about ensuring the highest standards in pharmaceuticals and vaccines, this is the perfect opportunity for you! Biological E Limited Hiring in Quality Assurance
Available Roles in Quality Assurance
Biological E. Limited is hiring for the following QA roles:
1. Executive / Senior Executive – DS-IPQA (In Process)
Responsibilities:
Handle cell or virus culture processes.
Prepare and maintain SOPs, BPRs, MFRs, and protocols.
Manage deviations, change control, and CAPA (Corrective and Preventive Action).
Ensure batch release, and maintain cell/viral bank systems.
Conduct cleaning and process validation. Biological E Limited Hiring in Quality Assurance
Candidates who have attended an interview with Biological E. Limited in the past 6 months or who have received an offer are requested not to attend this event.
If you are unable to attend, please send your CV to Careers@Biologicale.com.
Join Biological E. Limited and contribute to cutting-edge innovation in the pharmaceutical and vaccine industry!
Cell Engineering Scientist at Syngene International
Are you passionate about scientific innovation and cutting-edge cell engineering techniques? Syngene International, a leading contract research, development, and manufacturing organization (CRDMO), is seeking a talented Cell Engineering Scientist to join our dynamic team. This role is perfect for those who are eager to make an impact in the world of biotechnology, with hands-on experience in mammalian cell culture and stable cell line development. Whether you’re just starting out or looking to grow your expertise, this opportunity offers career growth and learning in a fast-paced environment. Cell Engineering Scientist at Syngene International
Why Syngene?
At Syngene, we are committed to creating a safe and responsible workplace that prioritizes safety alongside business performance. As a leader in innovation-driven scientific services, we provide integrated solutions across early discovery to commercial supply. Our company culture is rooted in Work/Life Balance, Time Management, and Flexibility, enabling employees to thrive professionally and personally. With global standards for Environment, Health, and Safety (EHS) in place, we ensure that safety is an integral part of our operations. Cell Engineering Scientist at Syngene International
Job Purpose
The Cell Engineering Scientist will play a crucial role in generating stable cell lines used in both research and production. As part of the Cell Engineering team, you’ll have the opportunity to contribute to the development of innovative tools and processes. This position provides valuable hands-on experience in molecular biology and advanced cell culture techniques, setting the stage for your professional growth in the biotechnology field. Cell Engineering Scientist at Syngene International
Key Responsibilities
Stable Cell Line Generation: Develop and maintain stable cell lines for production or research tools.
Cell Characterization: Use advanced techniques like flow cytometry and western blotting to analyze and characterize cell lines.
Experimentation & Planning: Design, plan, and conduct experiments. Analyze data, report findings, and provide scientific insights.
Documentation & Inventory Management: Maintain accurate records of experimental data and manage cell bank inventories for research and production.
EHS Compliance: Ensure strict adherence to environment, health, and safety (EHS) protocols. Participate in mandatory safety training to ensure compliance with safety standards. Cell Engineering Scientist at Syngene International
Educational Qualifications
M.Sc./M.Tech/Masters in Biology, Biotechnology, or any related life sciences field.
Ph.D. holders in related fields are also encouraged to apply.
Technical & Functional Skills Required
Mandatory:
Experience with stable cell line generation.
Expertise in generating lentivirus or retrovirus.
Preferred:
Experience with CRISPR-Cas9 or other genome editing technologies.
Knowledge of creating reporter cell lines.
Familiarity with molecular biology techniques and flow cytometry.
Experience in cell bank preparation and inventory management. Cell Engineering Scientist at Syngene International
Additional Skills
Strong attention to detail, especially in maintaining accurate documentation.
Excellent verbal and written communication skills.
Problem-solving skills, with the ability to design and execute experiments effectively. Cell Engineering Scientist at Syngene International
Experience Required
0-3 years of relevant experience in mammalian cell culture.
For postgraduate candidates, a minimum of 2+ years of relevant experience is required. Cell Engineering Scientist at Syngene International
Why Apply?
By joining Syngene International, you’ll become part of an organization that values innovation, safety, and excellence. As a Cell Engineering Scientist, you’ll have the chance to work with cutting-edge technology and contribute to projects that have a real-world impact. If you’re looking to advance your career in biotechnology while working in a supportive and growth-oriented environment, this is the perfect role for you! Cell Engineering Scientist at Syngene International
Ready to shape the future of cell engineering? Apply now to join our talented team at Syngene International!
Immuneel Therapeutics Hiring for Trainee QA Manufacturing Compliance
Location: Bangalore Experience: 0 Years (Freshers welcome!) Salary: Not Disclosed Education: M.Pharm, M.Tech Application Mode: Email
About Immuneel Therapeutics
Immuneel Therapeutics is leading the charge in cell and gene therapy to create transformative treatments for diseases like cancer. As pioneers in CAR-T and innovative therapies, Immuneel is focused on high-quality manufacturing and compliance. This is your opportunity to join a team that’s making a difference in patients’ lives. Immuneel Therapeutics Hiring for Trainee QA Manufacturing Compliance
Position Overview: Trainee QA (Manufacturing Compliance)
As a Trainee QA at Immuneel, you’ll support the manufacturing of life-saving products, ensuring they comply with the highest standards. This role is ideal for fresh graduates with a background in biopharmaceuticals and an eagerness to learn about quality assurance in cutting-edge biotech environments. Immuneel Therapeutics Hiring for Trainee QA Manufacturing Compliance
Key Responsibilities
In-Process Quality Assurance (IPQA): Monitor dispensing, area clearance, line clearance, and material reconciliation during production.
Batch Record Review: Assist in reviewing manufacturing batch records for CAR-T products and support Drug Substance (DS) and Drug Product (DP) batch releases.
Annual Product Quality Review (APQR): Help prepare documentation for APQR to ensure manufacturing compliance.
Audits and Inspections: Participate in internal audits and regulatory inspections, ensuring alignment with industry standards.
Collaboration: Work with QA and manufacturing teams to address deviations, out-of-spec (OOS) results, and conduct risk assessments.
Compliance Documentation: Maintain detailed and accurate records of all quality-related activities. Immuneel Therapeutics Hiring for Trainee QA Manufacturing Compliance
Desired Qualifications and Skills
Education: M.Pharm in Quality Assurance or M.Tech in Biopharmaceutical Technology/Biological Sciences.
Skills:
Strong interest in biotech and biopharmaceutical quality assurance.
Excellent attention to detail and organizational skills.
Basic knowledge of regulatory standards for cell and gene therapies.
Willingness to work in shifts, if required. Immuneel Therapeutics Hiring for Trainee QA Manufacturing Compliance
Why Join Immuneel?
Be part of a biotech company developing breakthrough therapies.
Gain hands-on experience in quality assurance and manufacturing compliance.
Work alongside industry experts in CAR-T and innovative therapies. Immuneel Therapeutics Hiring for Trainee QA Manufacturing Compliance
How to Apply
Ready to launch your career in biotech? Submit your application as follows:
Prepare your updated resume.
Email your profile to: careers@immuneel.com Subject line: “Application for Trainee QA (Manufacturing Compliance)”
Jumpstart your career in a transformative biotech field with Immuneel Therapeutics!
Netskope redefines Cloud, Network, and Data Security, creating a new perimeter built in the cloud to protect data wherever it goes. Founded in 2012, Netskope has grown into the market-leading cloud security company with an award-winning culture. Our offices are located in Santa Clara, St. Louis, Bangalore, London, Melbourne, Taipei, and Tokyo. Our core values are openness, honesty, and transparency, supported by our open desk layouts and large meeting spaces to foster collaboration and teamwork.
Job Information
Position Name: Staff Engineer Company Name: Netskope Department: Engineering Qualification: B.E/B.Tech/M.Tech degree from a recognized university/college Experience: Minimum 12+ years in the IT industry, with at least 5 years in DevOps and/or CI/CD Job Location: Multiple locations (Santa Clara, St. Louis, Bangalore, London, Melbourne, Taipei, and Tokyo) E-Mail: Not provided (Refer to Netskope Careers for application details)
Job Overview
We are seeking a Staff Engineer to join our team of experts to build applications that enhance engineering productivity at Netskope. This role is ideal for individuals driven by high-quality, high-velocity software delivery challenges and innovative solutions.
Develop and implement best-in-class CI/CD systems with cross-sectional engineering teams.
Design and code tools, applications, and dashboards to improve productivity.
Take complete ownership of work and mentor junior engineers.
Ensure CI/CD infrastructure is elastic, reliable, and resilient.
Preferred Qualifications
B.E/B.Tech/M.Tech degree from a recognized university/college.
Minimum 12+ years in the IT industry, with at least 5 years in DevOps and/or CI/CD.
Preferred Technical Skills
8+ years in building web/cloud scale applications using modern Web 2.0 technologies.
Solid understanding of Virtualization and Container technologies, with experience in Docker and Kubernetes.
4+ years of demonstrated Python/GoLang development experience.
Experience with database technologies such as MongoDB, MySQL, Postgres, or Cassandra.
Strong knowledge of automation tools such as Jenkins, Git, Jira, Spinnaker, and Ansible.
Expert-level understanding of Linux/Ubuntu.
Strong understanding of static code analysis, unit testing, test-driven development, security testing, and automated test frameworks.
Desired Technical Skills
Experience with frameworks like NodeJS, Angular, or Bootstrap.
Programming experience in Golang.
Additional Skills
Ability to multi-task and work on multiple project teams.
Strong written, verbal, and presentation skills.
Self-motivated with intellectual curiosity and a strong go-getter attitude.
Superior communication skills to articulate problems, solutions, risks, and rewards.
Analytical skills to identify gaps and areas of improvement in processes and technologies.
Equal Opportunity Employer
Netskope is committed to equal employment opportunities for all employees and applicants, and does not discriminate based on any characteristic protected by law. For more details, refer to Netskope’s Privacy Policy.
Meta Description:
Join Netskope as a Staff Engineer to enhance engineering productivity with cutting-edge solutions. Apply now for this dynamic role!
![[FRESHERS] Aurobindo Pharma Hiring for Manufacturing API](https://pharmabharat.com/wp-content/uploads/2024/11/ABL-1-724x1024.webp "[FRESHERS] Aurobindo Pharma Hiring for Manufacturing API")
