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Fresher Apotex Hiring for Trainee

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Fresher Apotex Hiring for Trainee
Fresher Apotex Hiring for Trainee

Company: Apotex Inc.
Position: Trainee – GBS-AGO
Location: Mumbai, Maharashtra, India
Experience: 0–1 year
Qualifications: B.Pharm, M.Pharm, MSc, BSc

About Apotex Inc.

Apotex Inc. is a leading global healthcare organization based in Canada, renowned for its commitment to delivering accessible, high-quality medicines. Operating in over 75 countries with a workforce of 7,200+ professionals, Apotex is a trusted name in generic, biosimilar, and specialty pharmaceutical products. Fresher Apotex Hiring for Trainee

Joining Apotex as a Trainee – GBS-AGO offers you the opportunity to develop your technical writing skills, collaborate with diverse teams, and contribute to global healthcare solutions. Fresher Apotex Hiring for Trainee

Role Overview

As a Trainee – GBS-AGO, you will manage and create technical documents that support Apotex’s manufacturing processes, ensuring compliance with regulatory standards and operational excellence.

Key Responsibilities

Document Creation and Management

  • Draft and format technical documents such as Technical Transfer Packages, Validation Reports, and Operational Reports.
  • Update and migrate Manufacturing Process and Packaging Records (MPPDs) into new templates (MMaR and MPaR).
  • Execute and cancel documents using the Content Server system.
  • Conduct peer reviews and oversee change control processes.

Compliance and Quality Assurance

  • Perform all tasks in alignment with Good Manufacturing Practices (GMPs) and Standard Operating Procedures (SOPs).
  • Adhere to Apotex’s core values: Courage, Passion, Perseverance, and Collaboration.

Team Collaboration and Support

  • Build strong relationships with internal and external customers.
  • Work collaboratively within a team to meet project deadlines and organizational goals.

Qualifications and Skills

Educational Background

  • Bachelor’s or Master’s degree in Pharmacy or Science.

Technical Skills

  • Proficiency in MS Office tools.
  • Familiarity with document management systems and online modules (preferred).

Soft Skills

  • Excellent written and verbal communication.
  • Strong multitasking and problem-solving abilities.
  • Adaptability in a dynamic work environment.

Why Join Apotex?

  • Gain hands-on experience in pharmaceutical technical documentation.
  • Work in a collaborative and supportive environment that fosters professional growth.
  • Be part of a global leader driving innovation and excellence in healthcare.

Start your career with Apotex Inc. and make an impact on global healthcare solutions!

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ICON plc Hiring for Internship

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ICON plc Hiring for Internship
ICON plc Hiring for Internship

Company: ICON plc
Location: Bengaluru, India
Experience: Freshers
Qualifications: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences, Business

About ICON plc

ICON plc is a global leader in healthcare intelligence and clinical research, recognized for its innovative work environment and commitment to advancing clinical development. With a strong focus on teamwork, diversity, and professional growth, ICON offers a dynamic platform for young professionals to learn and contribute meaningfully. ICON plc Hiring for Internship

Internship Overview

ICON plc is offering an internship program designed to provide hands-on experience in clinical research and healthcare intelligence. This is a unique opportunity to work on impactful projects and gain professional skills in a supportive and innovative environment. ICON plc Hiring for Internship

Key Responsibilities

  • Research and Data Analysis:
    Support ongoing projects by conducting research, collecting data, and performing analyses.
  • Team Collaboration:
    Participate in team meetings, share insights, and propose innovative solutions to enhance project outcomes.
  • Documentation and Reporting:
    Assist in preparing reports, presentations, and other project-related materials.
  • Administrative Support:
    Help streamline daily operational tasks to ensure efficient team functioning.
  • Professional Development:
    Engage in company-wide networking activities and training sessions to enhance your skillset.

Qualifications and Requirements

  • Educational Background:
    Pursuing or recently completed a Bachelor’s or Master’s degree in Life Sciences, Business, or a related field.
  • Learning Mindset:
    Keen interest in developing new skills and gaining practical experience in clinical research.
  • Communication Skills:
    Proficiency in written and verbal communication for effective collaboration.
  • Organizational Abilities:
    Strong time management and multitasking skills to handle various tasks efficiently.
  • Technical Proficiency:
    Familiarity with Microsoft Office applications; knowledge of data analysis or project management tools is a plus.

Skills to Excel

  • Critical Thinking: Analyze challenges and propose practical solutions.
  • Attention to Detail: Maintain accuracy in all assigned tasks.
  • Teamwork: Work effectively within diverse and dynamic teams.
  • Passion for Healthcare: Demonstrate enthusiasm for contributing to innovative healthcare solutions.

Why Join ICON plc?

  • Professional Growth: Gain hands-on experience and develop key industry skills.
  • Dynamic Environment: Work in an inclusive and innovative setting.
  • Meaningful Work: Contribute to advancing clinical development and healthcare intelligence.

Start your journey with ICON plc and make a meaningful impact in the world of clinical research!

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Fortrea Hiring for Safety Writer

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Fortrea Hiring for Safety Writer

Fortrea Hiring for Safety Writer

Company: Fortrea
Location: Pune, India
Experience: 1 – 3 Years
Salary: ₹4.5 – ₹6 LPA
Qualifications: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences

About Fortrea

Fortrea is a global leader in contract research, specializing in clinical development, patient access, and technology solutions. Operating across more than 90 countries with over 19,000 professionals, Fortrea supports pharmaceutical, biotechnology, and medical device companies in bringing life-saving treatments to patients worldwide. Renowned for its scientific excellence, Fortrea is dedicated to innovation and high-quality standards. Fortrea Hiring for Safety Writer

Role Overview

As a Safety Writer at Fortrea, you will be integral to the preparation of safety-related documents for global regulatory submissions. This includes authoring reports, conducting signal detection, and ensuring compliance with international regulatory requirements. Fortrea Hiring for Safety Writer

Key Responsibilities

  1. Authoring and Reviewing Reports:
    • Prepare Periodic Safety Update Reports (PSURs), Risk Management Plans (RMPs), and other safety-related documents.
    • Review safety data and reports to ensure clarity and compliance.
  2. Signal Detection:
    • Identify and evaluate potential risks associated with drugs or medical devices.
  3. Literature Searches:
    • Perform and analyze literature searches to support regulatory submissions.
  4. Supporting Documents:
    • Generate line listings, summary tabulations, and other supplemental documentation.
  5. Standard Operating Procedures (SOPs):
    • Create and review SOPs, Work Instructions (WIs), and process documentation.
  6. Training and Mentorship:
    • Provide guidance and training to team members on safety writing best practices.
  7. Regulatory Compliance:
    • Ensure that all documentation aligns with global regulatory standards (ICH, FDA, EMA).

Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Pharmaceutical Sciences, or related fields.
  • Experience in pharmacovigilance, safety writing, or regulatory writing within the pharmaceutical or clinical research industry.
  • Knowledge of global regulatory requirements (ICH guidelines, FDA regulations, EMA standards).

Skills Required

  1. Communication Skills: Strong writing ability to create clear and accurate safety reports.
  2. Analytical Thinking: Ability to assess data and identify safety risks effectively.
  3. Attention to Detail: Precision in reviewing and ensuring the accuracy of all documents.
  4. Team Collaboration: Comfortable working within cross-functional teams.
  5. Tool Proficiency: Familiar with safety reporting tools, literature databases, and MS Office applications.

Why Join Fortrea?

  • Work-Life Balance: Flexible schedules to promote well-being.
  • Global Impact: Contribute to life-saving treatments worldwide.
  • Career Growth: Opportunities to enhance skills and advance professionally.

Ready to make a difference? Apply now and join Fortrea in shaping the future of healthcare!

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Walk-In Drive Hiring for Women in STEM at Syngene

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Walk-In Drive Hiring for Women in STEM at Syngene

Walk-In Drive Hiring for Women in STEM at Syngene

Company: Syngene International Limited
Location: Gate No. 5, Velankani Tech Park, Electronics City Phase 1, Bengaluru, Karnataka
Position: Multiple Roles (Analyst, Scientist, Team Lead)
Experience: 2 – 15 Years
Educational Qualifications: MSc, M.Tech, M.Pharm, Master’s Degree in Molecular Biology or Genetics, Ph.D

About Syngene

Syngene International is a leading global biopharmaceutical company known for its innovative approach to science and technology. Recognizing the brilliance of women in STEM, Syngene is hosting a Walk-In Interview Drive to celebrate and empower women professionals in science, technology, engineering, and mathematics. This is an opportunity to join a workplace where your contributions make a global impact. Walk-In Drive Hiring for Women in STEM at Syngene

Walk-In Event Details

  • Date: 1st December 2024
  • Time: 9:00 AM to 12:30 PM
  • Venue: Syngene International Limited, Gate No. 5, Velankani Tech Park, Electronics City Phase 1, Bengaluru

Open Positions

  1. Purification Scientist – Req ID: 57784
  2. SPR Scientist – Req ID: 57670
  3. Cell Engineering Scientist – Req ID: 57532
  4. Assay Biologist – Req ID: 58134
  5. Molecular Biology Scientist – Req ID: 57053
  6. QC Analyst – Req ID: 58326
  7. Team Lead – Protein Purification – Req ID: 57007
  8. Molecular Biologist – Req ID: 58104
  9. Protein Purification Scientist – Req ID: 58426
  10. IPQC Reviewer – Req ID: 58070
  11. Target Dossier Analyst – Req ID: 57780

Why Join Syngene?

  • Cutting-Edge Technology: Work with state-of-the-art tools and technologies that push scientific boundaries.
  • Empowering Environment: Thrive in a dynamic and inclusive workplace celebrating diversity.
  • Global Impact: Contribute to healthcare and innovation with a worldwide influence.

What’s in Store for You?

  • Growth and leadership opportunities.
  • A meaningful role where your work directly impacts global healthcare.
  • An inclusive culture encouraging innovation, breaking barriers, and shattering glass ceilings.

Seize this chance to shape the future of science and technology!
Join Syngene to make a meaningful difference while advancing your career.

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Stanex Drugs and Chemicals Hiring for QC / QA

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Stanex Drugs and Chemicals Hiring for QC / QA

Company: Stanex Drugs and Chemicals Pvt Ltd
Location: IDA Cherlapally, Phase III, Plot No. 112, Hyderabad
Position: Quality Control (QC) & Quality Assurance (QA)
Experience: Freshers
Educational Qualifications: M.Pharm, B.Pharm, M.Sc (Analytical Chemistry)

About Stanex Drugs and Chemicals

Stanex Drugs and Chemicals Pvt Ltd is a leading pharmaceutical company in Hyderabad specializing in the manufacturing and development of high-quality drugs and chemicals. Known for its innovation, commitment to quality, and focus on employee development, the company is dedicated to meeting global pharmaceutical standards. Stanex Drugs and Chemicals Hiring for QC / QA

Interview Details

  • Date: 28th November 2024
  • Time: 10:00 AM
  • Venue: IDA Cherlapally, Phase III, Plot No. 112, Hyderabad

Roles & Responsibilities

Quality Control (QC)

  • Conduct testing and analysis of raw materials, in-process materials, and finished products.
  • Ensure compliance with safety, health, and regulatory standards.
  • Maintain accurate test records and report deviations or non-conformance.

Quality Assurance (QA)

  • Monitor quality control processes to ensure adherence to company policies and regulatory requirements.
  • Perform regular audits and inspections to maintain product quality.
  • Collaborate with the QC team to resolve quality issues and implement corrective actions.

Qualifications & Skills

Educational Requirements

  • M.Pharm, B.Pharm, or M.Sc in Analytical Chemistry from a recognized institution.

Skills

  • Strong understanding of pharmaceutical quality standards and regulatory guidelines.
  • Proficiency in laboratory testing techniques and equipment.
  • Attention to detail and accuracy in data recording.
  • Excellent communication and interpersonal abilities.

How to Apply

Interested candidates can attend the walk-in interview on 28th November 2024 at 10:00 AM.

Important Note:

  • Bring 4 original documents for submission during the interview.
  • A two-year mandatory bond is applicable for selected candidates.

Join Stanex Drugs and Chemicals to kickstart your career in pharmaceutical quality roles and contribute to delivering innovative healthcare solutions.

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Syneos Health Hiring for Clinical Data Associate II

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Syneos Health Hiring for Clinical Data Associate II

Location: Remote (India-Asia Pacific)
Experience Required: 1 – 4 Years
Salary: ₹4.5 – ₹7 Lacs per year
Educational Qualifications: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences

Why Join Syneos Health?

Syneos Health® is a globally recognized biopharmaceutical solutions leader with 29,000 employees across 110 countries. Dedicated to accelerating customer success, Syneos Health focuses on delivering therapies faster by combining clinical, medical affairs, and commercial expertise. With a strong commitment to innovation and improving lives, Syneos Health offers: Syneos Health Hiring for Clinical Data Associate II

  • Work/Life Balance
  • Flexibility
  • Opportunities for Growth
  • Dynamic Work Environment

About the Role: Clinical Data Associate II

As a Clinical Data Associate II (CDA II), you will play a vital role in managing data for clinical trials, ensuring accuracy, and streamlining processes.

Key Responsibilities

Data Management Tasks

  • Review and adhere to Clinical Data Management Plans specific to each study.
  • Perform User Acceptance Testing (UAT) for data entry screens and assigned data review listings.
  • Resolve discrepancies in clinical database entries and ensure accurate data submission.
  • Process Case Report Forms (CRFs) and Data Clarification Forms (DCFs).

Quality Control & Coordination

  • Conduct internal QC checks for both paper-based and Electronic Data Capture (EDC) studies.
  • Manage external datasets and ensure consistency across clinical databases.
  • Collaborate with other Clinical Data Associates (CDAs) and provide training as needed.

Other Responsibilities

  • Run data cleaning reports and reconcile Serious Adverse Events (SAEs).
  • Assist with interim data reviews and data cut processes.

Qualifications

Educational Requirements

  • BA/BS degree in biological sciences, healthcare, or natural sciences.

Experience

  • Prior experience in clinical research or data management preferred.
  • Knowledge of data management practices and relational database management software is a plus.

Preferred Skills

  • Familiarity with Oracle Clinical, Rave, or Inform systems.
  • Strong understanding of ICH/Good Clinical Practices and medical terminology.

Technical Skills

  • Proficiency in MS Windows, MS Word, Excel, and email applications.
  • Excellent keyboard skills with high speed and accuracy.

Soft Skills

  • Strong written and verbal communication skills.
  • Ability to manage multiple tasks, prioritize under tight deadlines, and work both independently and in teams.
  • Problem-solving skills to anticipate and address potential issues proactively.

Why This Role?

  • Work with a leading biopharmaceutical solutions organization.
  • Gain experience in innovative clinical trial processes.
  • Develop skills in managing critical data efficiently.

Apply Online Today to be part of Syneos Health and contribute to transforming healthcare solutions!

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Aurobindo Pharma Hiring for EHS

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Aurobindo Pharma Hiring for EHS

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:

  1. Staff
  2. Executive
  3. Assistant Manager (AM)
  4. Deputy Manager (DM)
  5. 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
  • Ensuring environmental monitoring (e.g., PCB management)

Why Join Aurobindo Pharma?

  • Work with a reputed pharmaceutical leader
  • Be part of cutting-edge safety and environmental practices
  • Contribute to critical API Division operations in Hyderabad

Walk-In Interview Details

Date: [Insert Date]
Time: [Insert Time]
Venue: Apitoria Pharma Private Limited, Hyderabad

Eligibility Criteria

  • Qualification: M.Tech / B.Tech / M.Sc / B.Sc in relevant fields
  • Experience: 2 to 15 years in EHS-related roles

Important Note

  • Apitoria Pharma does not charge any fees for job applications or processing.
  • Be cautious of scams or third-party invitations.

How to Apply

  • Step 1: Prepare your updated resume
  • Step 2: Attend the walk-in interview at the given venue in Hyderabad

For more details, you can contact the company directly.

Don’t miss the opportunity to join one of the leading pharmaceutical companies in the industry!

Keywords: Aurobindo Pharma, EHS Jobs, Environmental Health Safety, Pharmaceutical Jobs, Walk-In Interview, Hyderabad Jobs, API Division, Waste Management, Firefighting Systems, Safety Audits, Compliance.

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Freshers SCL Hiring for RD / ARD

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Freshers SCL Hiring for RD / ARD

Company: Saurav Chemicals Ltd

Experience: Freshers
Location: Derabassi, Punjab
Qualification: M.Sc. in Chemistry
Position: AR&D (Analytical Research & Development) and R&D (Research & Development)

About Saurav Chemicals Ltd

Established in the early 90s, Saurav Chemicals Ltd (SCL) is a leading manufacturer and supplier of Active Pharmaceutical Ingredients (APIs) and Intermediates globally, including in Europe, Japan, Russia, South & Central America, ASEAN, West Asia, and MENA regions. The company complies with EU GMP and U.S. FDA norms and is renowned for its expertise in pharmaceuticals trading and distribution. Freshers SCL Hiring for RD / ARD

Exciting Opportunity for Freshers in R&D and AR&D

Saurav Chemicals Ltd is hiring Freshers with a passion for chemistry to join their USFDA-approved API manufacturing facility in Derabassi, Punjab. The open positions are in the ARD (Analytical Research & Development) and R&D (Research & Development) departments. Freshers SCL Hiring for RD / ARD

Why Join Saurav Chemicals Ltd?

  • Work with a globally recognized API manufacturing leader.
  • Gain hands-on experience in state-of-the-art, USFDA-approved facilities.
  • Opportunity to contribute to pharmaceutical innovation in the ARD and R&D departments.

Walk-In Interview Details

Date: [Insert Date]
Time: [Insert Time]
Venue: Saurav Chemicals Ltd, Derabassi, Punjab

Eligibility Requirements

  • Qualification: M.Sc. in Chemistry
  • Experience: Freshers welcome to apply

How to Apply

Don’t Miss This Opportunity to Kickstart Your Career!
Join Saurav Chemicals Ltd and be part of an innovation-driven pharmaceutical company with a global presence. Apply today and start your journey in R&D and AR&D.

For Queries

Keywords: Saurav Chemicals, Walk-In Interview, R&D Jobs, AR&D Jobs, Pharmaceutical Jobs, API Manufacturing, Freshers Jobs, Chemistry Jobs, USFDA Facility, Derabassi, Punjab.

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Felix Generics Hiring for QC Production

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Felix Generics Hiring for QC Production
Felix Generics Hiring for QC Production

Company: Felix Generics

Experience: 1 – 11 years
Location: Pithampur Plant, Madhya Pradesh
Qualifications: M.Sc. / M. Pharma / B. Pharma / ITI / Diploma
Interview Date: 1st December 2024 (Sunday)
Time: 10:00 AM to 3:30 PM
Venue:
Lemon Tree Premier
Plot No. 2, Survey No. 64, HITEC City, Madhapur
Hyderabad, Telangana – 500081

Open Positions at Felix Generics

1. Quality Control (OSD)

Stability Section In-Charge
  • Experience: 10-11 years
  • Qualification: M.Sc. / M. Pharma / B. Pharma
  • Key Responsibilities:
    • Team management, work allocation, and resource management
    • Preparation and review of stability study protocols
    • Troubleshooting technical issues
    • Managing stability data, ANDA filings, and FAR
    • Drafting SOPs and preparing for regulatory inspections
QC Validation Officer to Executive
  • Experience: 3-8 years
  • Qualification: M.Sc. / M. Pharma / B. Pharma
  • Key Responsibilities:
    • Validation and qualification of laboratory equipment
    • Preparing documents for regulatory audits
    • Managing DR and OOS investigations
QC Sr. Officer to Executive
  • Experience: 4-8 years
  • Qualification: M.Sc. / M. Pharma / B. Pharma
  • Key Responsibilities:
    • Conducting analysis for RM/PM/In-process/FP samples
    • Managing analytical data for regulatory filings

2. Production (OSD)

Granulation/Compression/Packing Officer to Executive
  • Experience: 3-8 years
  • Qualification: B. Pharma / M. Pharma
  • Key Skills:
    • Experience in handling USFDA regulatory audits
    • Hands-on experience in granulation, tablet compression, and coating processes
    • Knowledge of SOPs and daily operations in pharmaceutical manufacturing
Granulation/Compression/Packing Technician
  • Experience: 1-5 years
  • Qualification: ITI / Diploma
  • Key Responsibilities:
    • Operating machinery for granulation and compression
    • Managing and maintaining primary and secondary packaging operations

Candidate Guidelines

  • Preference will be given to candidates with experience in USFDA-compliant regulated plants.
  • Interested candidates should bring the following documents:
    • Updated CV
    • Recent passport-size photograph
    • Latest pay slips

For Any Queries

Keywords: Felix Generics, Walk-In Interview, Quality Control Jobs, Production Jobs, OSD Manufacturing, Granulation, Compression, USFDA Compliance, Pharma Jobs, Stability Study, Regulatory Audits.

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Cipla Hiring for Production Manufacturing Packing and QA

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Cipla Hiring for Production Manufacturing Packing and QA

Cipla Hiring for Production Manufacturing Packing and QA

Company: Cipla

Experience: 1 – 5 years
Locations: Baddi, Goa, Sikkim & Other Sites
Qualifications: B.Pharm / M.Pharm / DPharm / DME / DEE
Interview Date: 1st December 2024
Time: 9:00 AM – 4:00 PM
Venue:
The Aures Hotel & Banquets
Padampura Circle, Station Road
Chh. Sambhaji Nagar (Aurangabad) 431005
Maharashtra, India

Available Positions

1. OSD Production – Operator

  • Job Role: Operating machines for Tablet, Capsule, and Ointment production.
  • Qualifications: DPharm / DME / DEE
  • Experience: 1 – 5 years

2. Sterile Manufacturing / Filling Operator

  • Job Role: Handling FFS, BFS, Autoclave, Steam Sterilizers, Filling & Sealing Machines (Bosch & Groninger), Ampoule & Vial Filling, and Injectable Manufacturing.
  • Qualifications: DPharm / DME / DEE
  • Experience: 1 – 5 years

3. OSD & Sterile Packing – Operator

  • Job Role: Operating packing lines for OSD & Sterile Manufacturing.
  • Qualifications: DPharm / DME / DEE
  • Experience: 1 – 5 years

4. Sterile Quality Assurance – Officer

  • Job Role: Expertise in IPQA, Validation, QMS, and EMQA sections.
  • Qualifications: B.Pharm / M.Pharm
  • Experience: 2 – 5 years

Eligibility Requirements

  • Pharma Manufacturing Experience: Candidates must have experience in regulatory-approved organizations (USFDA, MHRA, EU, etc.).
  • Apprentices Eligible: Candidates with more than 6 months of relevant experience can apply.

Documents to Carry

  • Updated Resume
  • Qualification Certificates & Marksheets
  • Current Company Appointment Letter
  • Latest Increment Letter
  • Last 3 Months’ Pay Slips
  • PAN Card & Aadhaar Card
  • 3 Passport-Sized Photographs

Unable to Attend the Walk-In?

Send your resume to ta.hr@cipla.com

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Keywords: Cipla Walk-In Interview, Pharma Jobs, Production Operator, Packing Operator, Sterile Manufacturing, Quality Assurance Officer, Pharma Manufacturing Jobs, OSD Production.