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Freshers Biotech Production Jobs at Covalent Laboratories, Apply on Biotecnika
Looking to begin your career in the pharmaceutical and biotechnology industry? Explore the latest Freshers Biotech Production Jobs at Covalent Laboratories, Apply on Biotecnika and discover excellent entry-level opportunities for biotechnology and life sciences graduates. These roles offer hands-on exposure to GMP-compliant production environments, documentation practices, and regulatory workflows—making them ideal for freshers aiming to build a strong foundation in biotech manufacturing.
Covalent laboratories
Company name: Covalent Laboratories
Job Title: Production
Experience: 0-6 Years
Location: Sangareddy, Telangana
Employment Type: full-time
Educational Qualification: B.Sc. Life Sciences, microbiology, biotechnology, B.Sc /
B.Pharmacy
Salary: ₹1.8–4.5 LPA for freshers; ₹3.5–8 LPA for experienced roles).
Attractive benefits include:
• Subsidized canteen facilities
• Attendance bonus
• Free transportation
Interview Mode: Walk-in interview
Job Summary:
Covalent Laboratories is seeking a Production Executive to support manufacturing operations by ensuring accurate preparation, review, and maintenance of GMP-compliant production documents. The role is ideal for freshers or candidates with up to 0-6 year of experience who are looking to build a career in pharmaceutical production documentation and regulatory compliance.
Roles & Responsibilities :
Preparation, issuance, review, and archival of Batch Manufacturing Records (BMR)
and Batch Packing Records (BPR)
• Ensure all production documents are maintained as per cGMP and company SOPs
• Assist in documentation related to deviations, change controls, CAPA, and incidents
• Coordinate with Production, QA, and QC teams for document corrections and
approvals
• Ensure timely closure of batch documents and support batch release activities
• Maintain document control registers and production logs
• Assist during internal audits, external audits, and regulatory inspections
• Support SOP drafting, revision, and training documentation
• Ensure data integrity, accuracy, and traceability in all production records
Requirements:
• Basic understanding of pharmaceutical production processes
• Knowledge of GMP, SOPs, and documentation practices
• Good written and verbal communication skills
• Strong attention to detail and documentation accuracy
• Willingness to work in shifts as per production requirements
• Ability to coordinate with cross-functional teams
• Familiarity with MS Word and Excel is preferred
Interview Mode: walk-in interview
Required Qualifications:
• B.Sc / M.Sc in Life Sciences, Chemistry, Pharmacy, or Biotechnology
• Diploma or certification in Pharmaceutical Documentation / GMP will be an added
advantage
• Freshers with internship or project experience in pharma production/documentation
are encouraged to apply
CLICK HERE TO APPLY ONLINE
