Pharma Jobs at BDR Pharmaceuticals Hiring Analytical Method Validation API Production Specialists at Luna Padra for USFDA regulated pharma facility.
About the Company
BDR Pharmaceuticals is a fast-growing Indian pharmaceutical company known for its strong presence in regulated markets and commitment to high-quality drug development and manufacturing. Over the years, BDR Pharma has built a solid reputation for delivering complex generic formulations, APIs, and specialty pharmaceutical products that meet global regulatory standards.
The company operates state-of-the-art manufacturing facilities designed to comply with international regulatory requirements, including USFDA norms. With a focus on innovation, compliance, and operational excellence, BDR Pharmaceuticals provides an environment where professionals can apply their technical expertise while continuously upgrading their skills in a competitive global pharma landscape. Hiring Analytical Method Validation API Production
As part of its expansion strategy, BDR Pharmaceuticals is strengthening its workforce at the Luna, Padra facility and inviting experienced pharmaceutical professionals to join its Analytical Method Validation, API Production, and API Documentation teams.
Job Details
- Company Name: BDR Pharmaceuticals
- Industry: Pharmaceutical / API Manufacturing
- Job Type: Full-Time, Permanent
- Experience Required: 1 to 12 Years (role dependent)
- Education Required: M.Sc, B.Pharma, M.Pharma
- Work Location: Luna, Padra
- Plant Type: USFDA-regulated manufacturing facility
- Hiring Mode: Direct application via email
Job Description
BDR Pharmaceuticals is hiring skilled professionals across analytical development and API production functions. These roles are ideal for candidates who have hands-on experience in regulated pharmaceutical environments and are familiar with compliance-driven operations.
The selected candidates will be responsible for analytical method validation, API manufacturing activities, and critical documentation processes. Working in a USFDA-compliant facility, employees will play a key role in maintaining data integrity, regulatory compliance, and operational efficiency. Hiring Analytical Method Validation API Production
This hiring initiative offers opportunities for both early-career professionals and experienced specialists looking to grow within a reputed pharmaceutical organization. Hiring Analytical Method Validation API Production
Skills / Qualifications
Educational Qualifications
- M.Sc (Chemistry or relevant discipline)
- B.Pharma
- M.Pharma
Technical & Professional Skills
- Strong understanding of pharmaceutical quality systems
- Knowledge of GMP, GLP, and regulatory compliance
- Hands-on experience in USFDA-regulated plants preferred
- Ability to prepare and review technical documentation
- Familiarity with analytical instruments and laboratory practices
- Good communication and coordination skills
- Strong attention to detail and data integrity principles
Key Responsibilities
Analytical Method Validation & Development (1–12 Years Experience)
- Perform analytical method validation and development activities
- Handle instruments such as HPLC, GC, and Dissolution apparatus
- Execute wet chemistry analysis as per approved protocols
- Ensure compliance with pharmacopeial and regulatory guidelines
- Prepare validation protocols, reports, and related documentation
- Support regulatory submissions and audit requirements
- Investigate analytical deviations and ensure corrective actions
- Maintain laboratory records in accordance with data integrity standards
Hiring Analytical Method Validation API Production
Production (API) – Junior Level (1–3 Years Experience)
- Support day-to-day API manufacturing operations
- Ensure accurate filling and verification of production documents
- Maintain Batch Manufacturing Records (BMRs)
- Handle equipment usage logbooks and cleaning records
- Perform weighing balance verification as per SOPs
- Follow GMP and safety guidelines during production activities
- Coordinate with QA and Engineering for smooth operations
Hiring Analytical Method Validation API Production
Production (API) – Documentation (7–8 Years Experience)
- Prepare and review SOPs, BMRs, and ECRs
- Handle documentation related to API manufacturing processes
- Manage and investigate OOS (Out of Specification) and OOT (Out of Trend) results
- Perform Gap Analysis to ensure regulatory compliance
- Support internal and external audits
- Ensure documentation accuracy and regulatory readiness
- Train junior staff on documentation and GMP practices
Candidate Profile & Qualifications
- Candidates must have a strong background in the pharmaceutical industry
- Experience with regulated market products is highly preferred
- Prior exposure to USFDA-approved plants will be an added advantage
- Ability to work in a compliance-driven manufacturing environment
- Willingness to work at the Luna, Padra facility
Hiring Analytical Method Validation API Production
Benefits / Perks
- Opportunity to work in a USFDA-regulated manufacturing facility
- Exposure to global regulatory standards and audits
- Professional and structured work environment
- Career growth opportunities within a growing organization
- Competitive compensation as per industry standards
- Skill enhancement through hands-on technical responsibilities
Hiring Analytical Method Validation API Production
Why You Should Join
BDR Pharmaceuticals offers a strong platform for pharmaceutical professionals who want to build or advance their careers in regulated markets. The company emphasizes quality, compliance, and continuous improvement, making it an ideal workplace for individuals who value technical excellence and professional integrity. Hiring Analytical Method Validation API Production
By joining BDR Pharma, employees gain exposure to advanced analytical techniques, complex API manufacturing processes, and international regulatory expectations. The Luna, Padra facility provides a stable and growth-oriented environment for professionals at different career stages. Hiring Analytical Method Validation API Production
How to Apply
Interested and eligible candidates can apply by sending their updated resume to the recruitment team:
Email: mrunali.uttekar@bdrpharma.com
Please mention the position you are applying for in the subject line of the email.
Work Location: Luna, Padra
FAQs
1. Who can apply for these roles?
Candidates with 1 to 12 years of relevant pharmaceutical industry experience and the required qualifications can apply.
2. Is USFDA experience mandatory?
USFDA plant experience is preferred but not mandatory for all roles. Candidates with regulated market exposure will be given priority.
3. Are these positions suitable for freshers?
No, these roles require prior industry experience ranging from 1 to 12 years.
4. What is the job location?
All positions are based at the Luna, Padra facility.
5. Is this a permanent job?
Yes, these are full-time permanent positions based on company norms and performance.
This hiring drive by BDR Pharmaceuticals is an excellent opportunity for analytical and API production professionals seeking long-term growth in a regulated pharmaceutical manufacturing environment. Hiring Analytical Method Validation API Production
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