Flagship Biotech International Pvt. Ltd. (FBIPL), a leading pharmaceutical company founded in 2008, specializing in the manufacture and export of high-quality injectables and formulations, is hiring for multiple positions at its facilities in Padra, Baroda (Divine Laboratories Pvt. Ltd. – DLPL) and Ranu, Baroda (FBIPL). With a presence in over 70 countries and manufacturing plants certified by USFDA, WHO-cGMP, EU(CE), and other global regulatory authorities, we are committed to affordable healthcare and stringent quality standards. Join our dynamic team to contribute to our mission of delivering innovative pharmaceutical solutions globally!

Why Join Flagship Biotech International?

Flagship Biotech, headquartered in Navi Mumbai, operates state-of-the-art manufacturing facilities in Tarapur, Navsari, Naroda, and Baddi, with a strong R&D focus on oncology, gastroenterology, neurology, and more. Benefits include:

Work in USFDA and WHO-cGMP approved facilities with global regulatory compliance
Opportunities to engage in diverse roles across Business Development, Quality Assurance (QA), Quality Control (QC), ADL Formulation, and CMS-Regulated Market
Be part of a company with a 3.5/5 employee rating for job security (based on limited reviews) and a global network in 70+ countries
Contribute to a portfolio of 400+ registered formulations and 700+ pharmaceutical products

Note: Limited employee feedback suggests a focus on quality but highlights challenges with work culture. Candidates should discuss career growth and work environment during interviews.

Available Positions

Below are the open positions at DLPL (Padra, Baroda) and FBIPL (Ranu, Baroda):

DLPL – Padra, Baroda

Location: Divine Laboratories Pvt. Ltd., 471, Dabhasa, Padra, Vadodara, Gujarat 391440

Executive – Business Development
- Department: Business Development
- Experience: 2–4 years
- Vacancy: 1
- Key Responsibilities:
  - Identify and develop new business opportunities in regulated markets
  - Coordinate with clients and manage sales pipelines
  - Prepare proposals and presentations for business pitches
- Required Skills:
  - Strong communication and negotiation skills
  - Knowledge of pharmaceutical markets (ROW preferred)
  - Proficiency in CRM tools and MS Office
Sales Coordinator – Tender
- Department: Tender
- Experience: 1–4 years
- Vacancy: 1
- Key Responsibilities:
  - Manage tender documentation and submission processes
  - Coordinate with internal teams for tender compliance
  - Maintain records of bids and client communications
- Required Skills:
  - Experience in tender management (pharma preferred)
  - Strong organizational and documentation skills
  - Familiarity with regulatory bidding processes
Assistant Manager – Quality Assurance
- Department: Quality Assurance
- Experience: 8–10 years
- Vacancy: 1
- Key Responsibilities:
  - Oversee QA processes, including batch release and documentation
  - Ensure compliance with cGMP, USFDA, and WHO guidelines
  - Conduct internal audits and manage QMS (CAPA, deviations)
- Required Skills:
  - Expertise in QA for injectables or OSD
  - Knowledge of regulatory audits (USFDA, EU-GMP)
  - Strong leadership and analytical skills
Senior Officer – Quality Control
- Department: Quality Control
- Experience: 3–5 years
- Vacancy: 1
- Key Responsibilities:
  - Perform analytical testing using HPLC, GC, UV, and FTIR
  - Conduct stability studies and method validation
  - Maintain QC documentation and data integrity
- Required Skills:
  - Hands-on experience with analytical instruments
  - Knowledge of cGMP and GLP
  - Familiarity with injectables testing

FBIPL – Ranu, Baroda

Location: Block No. 362/363/364, Ranu Village, Padra, Vadodara, Gujarat 391445

Senior Executive / Assistant Manager – Quality Assurance
- Department: Quality Assurance
- Experience: 7–10 years
- Vacancy: 1
- Key Responsibilities:
  - Lead QA activities, including process validation and line clearances
  - Review BMR, BPR, and SOPs for compliance
  - Support regulatory audits and CAPA implementation
- Required Skills:
  - Expertise in QA for regulated markets (USFDA, EU)
  - Strong knowledge of QMS and cGMP
  - Experience in injectables or biopharmaceuticals
Senior Manager – Quality Control (Chemical)
- Department: Quality Control (Chemical)
- Experience: 10–15 years
- Vacancy: 1
- Key Responsibilities:
  - Oversee chemical analysis of APIs and finished products
  - Manage method development, validation, and stability studies
  - Ensure compliance with USFDA and ICH guidelines
- Required Skills:
  - Advanced expertise in HPLC, GC, and spectroscopic techniques
  - Leadership in QC operations for regulated markets
  - Strong regulatory audit experience
Senior Manager – Quality Control (Microbiology)
- Department: Quality Control (Microbiology)
- Experience: 10–15 years
- Vacancy: 1
- Key Responsibilities:
  - Lead microbiological testing (sterility, BET, environmental monitoring)
  - Manage lab operations and ensure cGMP compliance
  - Oversee validation of microbiological methods
- Required Skills:
  - Expertise in microbiological testing for injectables
  - Knowledge of USP, EP, and regulatory standards
  - Experience with aseptic processes and audits
Officer to Senior Manager – Quality Assurance
- Department: Quality Assurance
- Experience: 2–14 years
- Vacancy: 1
- Key Responsibilities:
  - Perform IPQA, documentation, and validation activities
  - Support regulatory submissions and audits
  - Implement QMS processes (deviations, change controls)
- Required Skills:
  - Knowledge of cGMP and regulatory requirements
  - Experience in QA for injectables or OSD
  - Strong documentation and analytical skills
Senior Executive – ADL Formulation
- Department: Analytical Development Lab (ADL) Formulation
- Experience: 7–10 years
- Vacancy: 1
- Key Responsibilities:
  - Develop and validate analytical methods for formulations
  - Conduct stability studies and support scale-up
  - Prepare documentation for regulatory submissions
- Required Skills:
  - Expertise in HPLC, GC, and method development
  - Knowledge of ICH guidelines and cGMP
  - Experience with injectables or OSD formulations
Manager – CMS-Regulated Market
- Department: CMS-Regulated Market
- Experience: 10–15 years
- Vacancy: 1
- Key Responsibilities:
  - Manage contract manufacturing services for regulated markets
  - Coordinate with clients and ensure compliance with USFDA, EU-GMP
  - Oversee project timelines and quality deliverables
- Required Skills:
  - Experience in CMS operations for regulated markets
  - Strong project management and client communication skills
  - Knowledge of global regulatory requirements
Manager – Business Development (BD-Regulated Market)
- Department: Business Development (Regulated Market)
- Experience: 10–15 years
- Vacancy: 1
- Key Responsibilities:
  - Drive business growth in regulated markets (US, EU, etc.)
  - Develop strategic partnerships and manage key accounts
  - Prepare and negotiate contracts and proposals
- Required Skills:
  - Proven track record in pharma BD for regulated markets
  - Strong negotiation and market analysis skills
  - Familiarity with USFDA and EU regulatory frameworks

How to Apply

Email Application: Send your updated CV to hr3@flagshipbiotech.com, planthr@flagshipbiotech.com, or flagship@flagshipbiotech.com with the subject line “Application for [Position] – [Location]” (e.g., “Application for QA Assistant Manager – Padra”).

Flagship Biotech International Walk-In Interviews – Exciting Opportunities in Padra and Ranu, Baroda!

Documents Required:
- Updated resume
- Cover letter (optional, highlighting relevant experience)
- Latest increment letter and payslips (if applicable)
- Educational certificates
- Aadhar and PAN card copies
Note:
- Immediate joiners or candidates with short notice periods are preferred.
- Specify the position and location in your application.
- Candidates with experience in regulated markets (USFDA, EU-GMP) are prioritized.

Application Deadline

Applications are accepted on a rolling basis. Early submissions are encouraged due to limited vacancies.

Contact Us

Email: hr3@flagshipbiotech.com, planthr@flagshipbiotech.com, flagship@flagshipbiotech.com
Phone: +91-22-27781651/52/53/54, +91-7738899554, +91-6359418315
Website: www.flagshipbiotech.com
Locations:
- Padra, Baroda: Divine Laboratories Pvt. Ltd., 471, Dabhasa, Padra, Vadodara, Gujarat 391440
- Ranu, Baroda: Flagship Biotech International Pvt. Ltd., Block No. 362/363/364, Ranu Village, Padra, Vadodara, Gujarat 391445

Additional Information

Company Background: Founded in 2008, Flagship Biotech International Pvt. Ltd. is a small enterprise (MSME) with a global presence in 70+ countries, including Asia, Africa, Latin America, and Europe. Its facilities in Padra and Ranu, Baroda, are part of a network of WHO-cGMP and USFDA-approved plants manufacturing injectables, OSD, and specialty formulations. The company is known for its strong R&D and 400+ registered formulations.
Location Context:
- Padra, Baroda: Located 20 km from Vadodara city, Padra is an industrial hub with excellent connectivity via NH48 and Vadodara Railway Station (25 km). The DLPL facility is near Jambusar Road, a key pharma cluster.
- Ranu, Baroda: Ranu Village, 15 km from Padra, is part of the Vadodara industrial belt, accessible via NH48 and supported by robust infrastructure.
Employee Feedback: Limited reviews suggest a focus on quality and regulatory compliance but note challenges with work culture and career progression. The average salary for a Senior Officer is approximately ₹4,50,000 per year (industry estimate). Candidates should inquire about growth paths and work-life balance.
Regulatory Compliance: Facilities adhere to USFDA, WHO-cGMP, EU(CE), and other standards, with expertise in eCTD/CTD dossier preparation for regulated markets.

Join Flagship Biotech International Pvt. Ltd. and contribute to our mission of providing affordable, high-quality healthcare solutions worldwide. We look forward to welcoming talented professionals to our team! 🌍