Job Opportunity: Trainee – Quality Assurance, Production, and Regulatory Affairs
Job Summary
Lok-Beta Pharmaceuticals is seeking motivated and detail-oriented fresh graduates to join our team as Trainees. This position offers a unique entry-level opportunity for candidates to gain hands-on experience in core pharmaceutical operations, including Quality Assurance (QA), Production, Regulatory Affairs (RA), and Clinical Quality Assurance (CQA). We are committed to fostering professional growth and providing a comprehensive understanding of GMP-regulated manufacturing environments. This is an ideal role for individuals looking to build a long-term career in the pharmaceutical industry.
Job Overview
- Company: Lok-Beta Pharmaceuticals
- Positions: Trainee (QA / Production / RA / CQA)
- Locations: Thane (Atgaon) & Verna, Goa
- Experience: 0 Years (Freshers are encouraged to apply)
- Salary: ₹1.75 – ₹2.5 LPA
- Employment Type: Full-Time, Permanent
- Number of Openings: 4
Responsibilities
As a trainee, you will work closely with senior professionals to support daily operational tasks while adhering to strict industry standards. Your core responsibilities will include:
- Quality Assurance (QA): Support documentation processes, assist in maintaining SOP compliance, and participate in internal audit preparation.
- Production Operations: Assist in day-to-day manufacturing activities, ensuring all processes remain aligned with Good Manufacturing Practices (GMP).
- Regulatory Affairs (RA): Provide support for regulatory documentation, assist in the preparation of submissions, and ensure alignment with regulatory filing requirements.
- Clinical Quality Assurance (CQA): Contribute to CQA activities to ensure data integrity and clinical compliance.
- Compliance & Documentation: Maintain accurate, real-time records of all activities and assist in validation processes to ensure the facility meets international ICH and GMP standards.
Eligibility Criteria
To be considered for this role, candidates must meet the following educational and professional requirements:
- Education: B.Pharm, M.Pharm, or B.Sc/M.Sc in Chemistry or related scientific disciplines.
- Experience: This is a dedicated fresher role; no prior industry experience is required.
- Core Competencies: A strong academic interest in pharmaceutical manufacturing, quality control, and regulatory frameworks is essential.
- Skills: A basic understanding of GMP guidelines, quality assurance processes, and pharma compliance is considered a significant advantage.
- Mindset: We are looking for candidates who are eager to learn, detail-oriented, and capable of working in a disciplined manufacturing environment.
Why Join Lok-Beta Pharmaceuticals?
Choosing a career at Lok-Beta Pharmaceuticals allows you to:
- Jumpstart Your Career: Gain entry into a competitive and rewarding core pharmaceutical sector.
- Cross-Functional Exposure: Obtain practical, hands-on experience across multiple departments, including QA, Production, and Regulatory Affairs.
- Professional Development: Operate within a professional, GMP-regulated manufacturing setup that prioritizes quality and safety.
- Growth Potential: Benefit from a structured environment that provides a clear trajectory for advancement within the pharmaceutical quality and regulatory domains.
How to Apply
We invite interested and qualified candidates to apply for these trainee positions by submitting an updated copy of their Curriculum Vitae (CV).
Application Instructions:
- Please send your updated resume to our hiring team via the official recruitment channel.
- Subject Line Requirement: To ensure your application is processed promptly, please use the subject line: “Trainee Application – QA/RA/Production.”
We look forward to reviewing your application and potentially welcoming you to the Lok-Beta Pharmaceuticals team.