Job Tag: Pharma Jobs in Pune

  • TL Pharmacovigilance Vacancy – Cognizant Associate Returnship Program

    TL Pharmacovigilance Vacancy – Cognizant Associate Returnship Program

    TL Pharmacovigilance Vacancy for Pharma Professionals in Pune

    Cognizant hiring TL Pharmacovigilance role in Pune. 6-9 years experience required. Apply now for full-time hybrid role.


    Cognizant, a global leader in digital transformation and professional services, is inviting applications for the position of Team Lead – Pharmacovigilance in Pune, India. This is a full-time, hybrid opportunity under the Associate Returnship Program. If you are an experienced pharma professional with strong expertise in Pharmacovigilance, Case Processing, and Pharma R&D, this role could be your next career milestone.


    Company Overview

    Cognizant is one of the world’s leading professional services companies, helping clients modernize their business, operations, and technology models for the digital era. Headquartered in the U.S., Cognizant is a NASDAQ-100 company and consistently recognized among Forbes World’s Best Employers. With a strong commitment to innovation, inclusivity, and employee growth, Cognizant is a trusted name in the global life sciences and healthcare services sector.


    Job Role & Responsibilities

    As TL – Pharmacovigilance, you will play a crucial role in ensuring drug safety, compliance, and regulatory adherence. Your responsibilities will include:

    • Overseeing pharmacovigilance activities in line with global regulatory requirements.
    • Leading safety operations with a focus on PV Case Processing.
    • Utilizing MS Excel for data reporting and safety analysis.
    • Monitoring and evaluating adverse event reports to identify potential safety signals.
    • Ensuring timely case processing and compliance with SOPs.
    • Coordinating with cross-functional and global teams for safety data integration.
    • Preparing regulatory safety reports and submissions.
    • Conducting audits, compliance checks, and continuous improvement initiatives.
    • Training and mentoring junior staff in pharmacovigilance operations.

    Eligibility / Qualifications

    • Education: M. Pharmacy, B. Pharmacy, Pharm.D, M.Sc Clinical Research, or related life sciences degrees.
    • Experience: 6 to 9 years in Pharmacovigilance, Safety Operations, or Pharma R&D.
    • Skills:
      • Strong proficiency in MS Excel.
      • Experience in PV Case Processing and Safety Ops preferred.
      • Excellent communication and cross-team collaboration skills.
    • Certifications: Certified Pharmacovigilance Professional (CPP) or equivalent preferred.
    • Work Model: Hybrid, with rotational shifts.

    Location & Salary

    • Location: Pune, India
    • Work Model: Hybrid
    • Employment Type: Full-time
    • Compensation: Competitive (as per company norms and experience)
    TL Pharmacovigilance Vacancy for Pharma Professionals - Cognizant Associate Returnship Program
    TL Pharmacovigilance Vacancy for Pharma Professionals – Cognizant Associate Returnship Program

    Application Process

    Candidates can apply directly through Cognizant’s official career portal:
    Apply Here

    Early applications are encouraged to secure your spot.


    Why Join Cognizant?

    • Work with a global team of 300,000+ associates.
    • Access continuous learning and career development.
    • Be part of a company recognized for innovation, inclusivity, and sustainability.
    • Opportunity to contribute directly to patient safety and drug development.

    FAQs

    Q1: What is the required experience for this role?
    A minimum of 6 to 9 years in Pharmacovigilance or Pharma R&D.

    Q2: Is this position suitable for freshers?
    No, this role requires prior experience in PV and safety operations.

    Q3: What certifications will add value to my application?
    A Certified Pharmacovigilance Professional (CPP) or equivalent certification is preferred.

    Q4: What is the work model for this position?
    This is a hybrid role with rotational shifts.

    Q5: How do I apply?
    You can apply online through Cognizant’s official careers portal.


    Summary Table

    Category Details
    Company Cognizant
    Vacancies 01
    Required Education M. Pharmacy, B. Pharmacy, Pharm.D, M.Sc Clinical Research, Life Sciences
    Experience 6–9 years in Pharmacovigilance, Case Processing, Pharma R&D
  • Macleods Pharmaceuticals Walk-In 100+ (QC, QA, Production)

    Macleods Pharmaceuticals Walk-In 100+ (QC, QA, Production)

    Macleods Hiring QC, QA & Production | 100+ Vacancies | Pune Walk-In

    Macleods Pharma hiring QC, QA & Production professionals. 100+ vacancies. Walk-in at Pune. Apply with B.Pharm/M.Pharm/M.Sc/B.E./Diploma qualifications.


    Macleods Pharmaceuticals Ltd., one of India’s leading pharma companies, is conducting a mega walk-in drive at Pune for Quality Control, Quality Assurance, and Production roles across its OSD and API facilities. With over 100+ vacancies, this is an excellent opportunity for pharma professionals seeking career growth in a globally trusted pharmaceutical organization.


    Company Overview

    Macleods Pharmaceuticals is a globally recognized pharma giant with strong footprints in over 140 countries. Known for its high-quality formulations and active pharmaceutical ingredients (APIs), the company is committed to innovation, regulatory compliance, and patient care. With multiple USFDA, WHO-GMP, and EU-approved facilities, Macleods continues to expand its workforce to meet growing international and domestic demands.


    Job Role & Responsibilities

    Openings are available across multiple departments, including Quality Control (OSD & API), Quality Assurance, and Production API.

    Quality Control (General OSD & API)

    • Conduct raw material, finished product, stability, and packing material analysis.
    • Perform analytical method validation (AMV) and analytical method transfer (AMT).
    • Hands-on experience in HPLC, GC, LCMS, PSD, and other analytical instruments.

    Quality Assurance (API & OSD)

    • Review of documents including BMR, SOPs, and QMS-related tasks.
    • Handle market complaints, deviations, CAPA, and change control.
    • Exposure to regulatory audits like USFDA, MHRA, WHO.

    Production (API)

    • Responsible for manufacturing processes of APIs and intermediates.
    • Ensure compliance with GMP guidelines during production operations.
    • Maintain safety standards and SOP adherence.

    Eligibility / Qualifications

    • Education: B.Sc., M.Sc. (Chemistry), B.Pharm, M.Pharm, B.E./B.Tech (Chemical), Diploma (Chemical).
    • Experience: 2–8 years depending on role.
    • Special Skills: Strong technical knowledge, experience in OSD/API facilities, and regulatory exposure.

    Courses covered: Organic Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, Industrial Chemistry, Chemical Engineering, Pharmacy (B.Pharm/M.Pharm).


    Location & Walk-In Details

    Candidates must bring: Updated CV, educational certificates, last 2 months’ payslips, increment letter, and ID proof.


    Application Process

    1. Scan the QR code or register online via the official Macleods Careers Portal.
    2. Attend the walk-in interview at the specified venue.
    3. Shortlisted candidates will be provided offer letters post-interview.

    Employee Benefits

    • Competitive salary packages.
    • PF, ESI, Bonus & Incentives.
    • Career progression opportunities across global units.
    • Training and exposure to international regulatory audits.

    FAQs

    Q1. Who can apply for Macleods Pune walk-in drive?
    Candidates with 2–8 years of experience in QC, QA, or Production with B.Sc., M.Sc., B.Pharm, M.Pharm, or B.Tech qualifications.

    Q2. Is prior pharma experience mandatory?
    Yes, experience in pharmaceutical OSD/API manufacturing and QC/QA roles is required.

    Q3. What should I carry for the walk-in interview?
    Updated CV, academic certificates, ID proof, payslips (last 2 months), and increment letter.

    Q4. Will freshers be considered?
    No, this walk-in is for experienced professionals only.

    Q5. Which locations are hiring apart from Pune?
    Other openings are available at Daman, Indore, Dahej, and Sarigam units.


    Summary Table

    Company Macleods Pharmaceuticals Ltd.
    Vacancies 100+ (QC, QA, Production)
    Required Education B.Sc., M.Sc., B.Pharm, M.Pharm, B.E./B.Tech, Diploma
    Experience 2–8 years
    Location Pune (also Daman, Indore, Dahej, Sarigam)
    Walk-In Date 28th August 2025
    <img class="size-full wp-image-123114" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Macleods-Pharma-Walk-in-100-QC-QA-Production-1.webp" alt="Macleods Pharma Walk-in 100+ (QC, QA, Production)” width=”720″ height=”960″ /> Macleods Pharma Walk-in 100+ (QC, QA, Production)
  • Akriti Pharma Hiring Plant Head/Production Head

    Akriti Pharma Hiring Plant Head/Production Head

    Plant Head Vacancy | B.Pharm/M.Pharm | Akriti Pharma Pune

    Akriti Pharma hiring Plant Head/Production Head in Jejuri, Pune. B.Pharm/M.Pharm with 15–20 yrs’ manufacturing & regulatory audit experience.


    Akriti Pharmaceuticals Pvt. Ltd., a EU-certified pharmaceutical formulation company, is urgently hiring for the position of Plant Head / Production Head at its state-of-the-art facility in Jejuri, Pune. This role is ideal for highly experienced pharma professionals seeking leadership opportunities in a globally certified company.


    Company Overview

    Akriti Pharmaceuticals Pvt. Ltd. is a reputed pharma formulation company, recognized for its expertise in manufacturing tablets, capsules, ointments, and dry powder injectables. With stringent compliance to international quality standards, including MHRA, USFDA, and EU certifications, Akriti Pharma is a trusted partner for domestic and global markets. The company emphasizes innovation, operational excellence, and regulatory compliance to deliver world-class medicines.


    Job Role & Responsibilities

    Position: Plant Head / Production Head
    Experience: 15–20 years
    Location: Jejuri, Pune

    Key Responsibilities:

    • Oversee daily manufacturing operations across tablet, capsule, ointment, and injectable plants.
    • Ensure smooth functioning of production activities with strict adherence to GMP guidelines.
    • Lead cross-functional teams to achieve production targets, efficiency, and quality compliance.
    • Handle regulatory audits from MHRA, USFDA, EU, and other international authorities.
    • Develop and implement SOPs for manufacturing excellence and compliance.
    • Report to senior management and contribute to strategic decision-making for plant operations.

    Eligibility / Qualifications

    • Education: B.Pharm / M.Pharm
    • Experience: 15–20 years in pharma manufacturing (tablets, capsules, ointments, dry powder injectables).
    • Skills Required:
      • Strong leadership and team management abilities.
      • Hands-on experience in facing regulatory audits (MHRA, USFDA, EU).
      • In-depth knowledge of GMP, production planning, and quality compliance.

    Location & Salary

    • Work Location: Jejuri, Pune (Maharashtra)
    • Job Type: Full-time (Leadership role)
    • Salary: Attractive package based on experience and qualifications.

    Application Process

    Interested candidates can share their updated CV to:

    Applicants are encouraged to apply immediately to secure this senior leadership opportunity.


    FAQs

    1. Who can apply for the Plant Head position at Akriti Pharma?
    Pharma professionals with B.Pharm/M.Pharm and 15–20 years of experience in formulations manufacturing.

    2. What products does the plant manufacture?
    Tablets, capsules, ointments, and dry powder injectables.

    3. Is regulatory audit experience mandatory?
    Yes, candidates must have prior exposure to audits from MHRA, USFDA, EU, or equivalent authorities.

    4. Where is the job located?
    The position is based at Jejuri, Pune (Maharashtra).

    5. How to apply?
    Send your CV to hrhead@akritipharma.com or resume@akritipharma.com with the subject line Application for Plant Head.


    Apply now and take on a leadership role at Akriti Pharmaceuticals’ EU-certified plant in Pune!


    Summary Table

    Company Akriti Pharmaceuticals Pvt. Ltd.
    Vacancies Plant Head / Production Head
    Required Education B.Pharm / M.Pharm
    Experience 15–20 years in pharma manufacturing & audits
  • Centaur Pharmaceuticals walk-in Production, QC, QA

    Centaur Pharmaceuticals walk-in Production, QC, QA

    Walk-In Interview for Experienced B.Pharm/M.Pharm, M.Sc Professionals | Centaur Anna Taffy is marriedPune

    Attend Centaur Pharma walk-in at Pune on 24th August 2025. Hiring experienced candidates for Production, QC, QA roles in OSD manufacturing facility.


    Are you an experienced pharma professional seeking to build your career with a USFDA and MHRA-approved facility? Centaur Pharmaceuticals Pvt. Ltd. is conducting a walk-in interview on 24th August 2025 (Sunday) at its Oral Solid Dosage (OSD) manufacturing plant in Pune. This is a golden opportunity for skilled candidates with experience in production, quality control, and quality assurance to join a company known for its compliance-driven culture and strong presence in the regulated markets.

    Company Overview

    Centaur Pharmaceuticals Pvt. Ltd. is one of the fastest-growing pharmaceutical companies in India, with a strong track record of compliance, innovation, and global market penetration. With manufacturing facilities approved by USFDA, MHRA, and EU regulators, Centaur has established itself as a trusted partner in the global pharmaceutical supply chain. The company focuses on Oral Solid Dosage (OSD) manufacturing and is committed to delivering high-quality, affordable medicines to patients worldwide. Joining Centaur means being part of a team that contributes directly to global healthcare advancement.

    Job Role & Responsibilities

    Centaur is hiring for multiple positions in its Production, Quality Control (QC), and Quality Assurance (QA) departments. The roles require prior exposure to regulatory audits (USFDA, MHRA, EU) and experience in formulation manufacturing companies.

    Production Department

    • Executive/Sr. Executive (Granulation, Compression, Coating, Packing, Investigations, QMS, Audit compliance).
      • Experience: 10–14 Years
      • Qualification: B. Pharm / M. Pharm
    • Officer/Sr. Officer (Granulation, Compression, Packing).
      • Experience: 6–8 Years
      • Qualification: B. Pharm / M. Pharm
    • Operator (Compression – AWC, Blister – BQC/PG-230 XT, Cartonator – Hi Cart IC150C, Strip Operator).
      • Experience: 5–10 Years
      • Qualification: ITI / B.Sc / D.Pharm / DME
      • Multi-skilled operators preferred.
      • Knowledge required: Machine troubleshooting, changeover, GMP, and Data Integrity.

    Quality Control Department

    • Officer/Sr. Officer (RM, In-process & FP, Stability, AMV & AMT, GLP, QMS, PM, Microbiology).
      • Experience: 4–8 Years
      • Qualification: M.Sc
    • Executive/Sr. Executive (AMV/AMT/RM/PM).
      • Experience: 6–10 Years
      • Qualification: B. Pharm / M. Pharm / M.Sc
    • Asst. Manager (RM, Stability, Microbiology).
      • Experience: 10–15 Years
      • Qualification: B. Pharm / M. Pharm / M.Sc

    Quality Assurance Department

    • Executive/Sr. Executive (QMS, AQA – Investigations).
      • Experience: 8–10 Years
      • Qualification: B. Pharm / M. Pharm / M.Sc
    • Sr. Officer/Executive/Sr. Executive (Validation, IPQA, CSV, ITQA).
      • Experience: 6–10 Years
      • Qualification: B. Pharm / M. Pharm

    Eligibility / Qualifications

    • Educational Background: B.Pharm, M.Pharm, M.Sc (Chemistry, Microbiology, Analytical Chemistry), ITI, D.Pharm, DME.
    • Experience Required: 4 to 15 years, depending on role.
    • Mandatory: Prior experience in formulation manufacturing (OSD) with exposure to USFDA, MHRA, or EU audits.

    Relevant Courses Include: B.Pharm, M.Pharm (Pharmaceutics, Pharmaceutical Technology, Quality Assurance), M.Sc (Analytical Chemistry, Microbiology, Industrial Chemistry), ITI Mechanical, D.Pharm.

    Location & Salary

    • Work Location: Centaur Pharmaceuticals Pvt. Ltd., Plot No. 4, International Biotech Park, Hinjewadi, Phase II, Pune – 411057.
    • Salary: Competitive and based on experience.
    • Interview Date & Time: 24th August 2025 (Sunday), 09:30 AM – 04:00 PM.

    Application Process

    Interested candidates with relevant experience are invited to attend the walk-in interview directly at the venue.

    Venue: Centaur Pharmaceuticals Pvt. Ltd., OSD Manufacturing Facility, Plot No. 4, International Biotech Park, Hinjewadi, Phase II, Pune – 411057.
    Date & Time: 24th August 2025 (Sunday), 09:30 AM – 04:00 PM.

    Documents to Carry:

    • Updated Resume.
    • Recent passport-size photograph.
    • Academic and experience certificates.

    Email for CV Submission: hrdeskpune@centaur.co.in
    Contact Number: +91-20-66739510

    Apply before 24th August 2025 and attend the walk-in to secure your opportunity with Centaur Pharmaceuticals!


    FAQs

    1. Who is eligible to apply for Centaur Pharma’s walk-in interview?
    Experienced candidates with 4–15 years in OSD manufacturing, QC, or QA, and exposure to USFDA/MHRA/EU audits.

    2. Can freshers apply?
    No, this recruitment drive is strictly for experienced candidates.

    3. What documents should I bring to the interview?
    Resume, passport-size photograph, and all academic and experience certificates.

    4. What type of facility is Centaur hiring for?
    The Pune facility specializes in Oral Solid Dosage manufacturing for regulated markets.

    5. Is regulatory audit exposure mandatory?
    Yes, prior exposure to USFDA, MHRA, or EU audits is compulsory.

    6. Can I send my resume by email?
    Yes, resumes can be sent to hrdeskpune@centaur.co.in.


    Summary Table

    Company Centaur Pharmaceuticals Pvt. Ltd.
    Vacancies Production, QC, QA (Multiple Roles)
    Required Education B.Pharm, M.Pharm, M.Sc (Chemistry, Microbiology, Analytical Chemistry), ITI, D.Pharm, DME
    Experience 4–15 Years (OSD manufacturing, USFDA/MHRA/EU exposure mandatory)
    Location Hinjewadi, Phase II, Pune, Maharashtra
    Walk-In Date 24th August 2025 (Sunday)
    Timing 09:30 AM – 04:00 PM
    Email hrdeskpune@centaur.co.in
    Contact +91-20-66739510
    Centaur Pharmaceuticals walk-in Production, QC, QA
    Centaur Pharmaceuticals walk-in Production, QC, QA
  • Synergen Bio Hiring 3 Trainee Research Associate

    Synergen Bio Hiring 3 Trainee Research Associate

    Trainee Research Associate Openings at Synergen Bio Pune | 3 Vacancies

    Apply now for 3 Trainee Research Associate vacancies at Synergen Bio, Pune. Open for MBA, B.Pharm, M.Pharm freshers and immediate joiners.


    Synergen Bio is inviting applications from freshers and early career professionals for the role of Trainee Research Associate in the Project Management and Biopharmaceutical department. With a reputation for excellence in Contract Research Organization (CRO) services, Synergen Bio offers candidates a chance to build a strong career foundation in clinical research and pharmaceutical project management.


    Company Overview

    Synergen Bio is a leading pharmaceutical and biopharmaceutical company that specializes in research, development, and CRO services. With a client-focused approach, the organization contributes significantly to the healthcare and life sciences sector by delivering high-quality research and development solutions. Known for its commitment to innovation and compliance, Synergen Bio provides an excellent platform for freshers to gain industry exposure and practical experience.


    Job Role & Responsibilities

    As a Trainee Research Associate, selected candidates will be responsible for supporting project management and biopharmaceutical operations. Key responsibilities include:

    • Providing client support for CRO services.
    • Acting as a communication link between project personnel and sponsors to resolve queries.
    • Monitoring and ensuring project deliverables meet agreed timelines and quality standards.
    • Coordinating with cross-functional teams for clinical research project development.
    • Planning, monitoring, and controlling different project phases, reporting progress to management.
    • Preparing service agreements and handling confidential documents.
    • Reviewing and drafting Standard Operating Procedures (SOPs).
    • Supporting regulatory documentation, including DCGI NOC submissions for BA/BE studies.
    • Performing additional tasks as delegated by the Head of Project Management and Biopharmaceutics.

    Eligibility / Qualifications

    Candidates must meet the following criteria:

    • Qualification: MBA, B.Pharm, M.Pharm (including courses like MBA in Pharmaceutical Management, B.Pharmacy, M.Pharmacy in Pharmaceutics/Pharmaceutical Analysis, Pharmacology, etc.)
    • Experience: 0 to 1+ years (freshers encouraged to apply).
    • Immediate joiners will be preferred.

    Location & Salary

    • Job Location: Pune, Maharashtra
    • Salary: As per industry standards and candidate profile.

    Application Process

    Interested candidates can share their updated CV with Synergen Bio’s HR team at:

    Email: careers@synergenbio.com


    FAQs

    1. Who can apply for this role?
    MBA, B.Pharm, and M.Pharm graduates (freshers and up to 1 year of experience) are eligible.

    2. Is prior clinical research experience required?
    No, freshers are welcome. However, candidates with internship or project exposure will have an added advantage.

    3. What is the work location?
    The position is based at Synergen Bio, Pune.

    4. Are immediate joiners preferred?
    Yes, candidates who can join immediately will be given priority.

    5. How can I apply?
    Send your CV to careers@synergenbio.com.


    Summary Table

    Company Synergen Bio
    Vacancies 03
    Required Education MBA, B.Pharm, M.Pharm
    Experience 0 to 1+ Years
    Location Pune, Maharashtra
    Synergen Bio Hiring 3 Trainee Research Associate
    Synergen Bio Hiring 3 Trainee Research Associate