APDM Pharmaceuticals, a leader in pharmaceutical innovation, is hosting a walk-in interview on September 16, 2025, from 9:30 AM to 4:30 PM at its facility in Sakodara, Ahmedabad. We are seeking skilled professionals for Warehouse Manager, Quality Control (Officer/Sr. Officer, Executive/Sr. Executive), and Production (Operator, Officer/Executive) roles. Candidates with experience in cGMP, regulatory audits (USFDA, EU, MHRA, ANVISHA), and pharmaceutical operations are encouraged to apply. Join a dynamic team dedicated to creating a healthy future at APDM Pharmaceuticals!
Job Roles and Responsibilities
1. Warehouse Manager
- Oversee receipt, sampling, storage, and issuance of raw materials (RM), packing materials (PM), and finished goods (FG).
- Ensure material handling per SOPs and cGMP requirements (quarantine, approved, rejected, returned, expired).
- Maintain FIFO/FEFO systems and traceability of materials.
- Coordinate with production, QA, QC, and purchase for timely material availability.
- Ensure compliance during regulatory inspections (USFDA, EU, MHRA, WHO).
- Handle deviations, OOS, change controls, and CAPAs.
- Monitor stock levels to avoid overstocking or stock-outs, conducting physical stock verification.
- Analyze slow-moving, near-expiry, and obsolete materials, taking corrective actions.
- Maintain warehouse equipment (weighing balances, forklifts, temperature/humidity systems).
- Ensure audit-ready conditions and implement corrective actions post-audits.
2. Quality Control (Officer/Sr. Officer, Executive/Sr. Executive)
- Ensure compliance with cGMP, GLP, GDP, and SOPs in the QC laboratory.
- Perform analysis and release of raw materials, packing materials, in-process, and finished products.
- Handle laboratory QMS activities (Change Control, Deviation, OOS, OOT, Incidents).
- Conduct AMV, method verification, and method transfer activities.
- Manage calibration of laboratory instruments and coordinate with service providers.
- Procure chemicals, standards, columns, and consumables timely.
- Review and execute technology transfer documentation.
- Develop QC strategies aligned with regulatory guidelines (USFDA, EU, MHRA, ANVISHA).
3. Production (Operator, Officer/Executive)
- Operator (Compression):
- Operate and monitor compression machines for tablet manufacturing.
- Ensure proper machine setup, changeover, and shutdown per SOPs.
- Adjust machine parameters to maintain product quality and yield.
- Perform line clearance and in-process checks (weight, thickness, hardness, friability, disintegration).
- Record activities in BMR and logbooks, adhering to cGMP and safety norms.
- Officer/Executive:
- Execute production schedules and coordinate with stores, QA, QC, engineering, and planning.
- Ensure timely availability of raw materials and consumables.
- Maintain compliance with cGMP, SOPs, and regulatory requirements (USFDA, EU, MHRA, WHO).
- Review BMRs, BPRs, and logbooks, handling deviations, change controls, and CAPAs.
Qualifications
- Warehouse Manager:
- Education: B.Pharm, M.Pharm, B.Sc, or M.Sc.
- Experience: 6–9 years in pharmaceutical warehouse management.
- Skills: Expertise in cGMP, FIFO/FEFO, inventory management, regulatory audits (USFDA, EU, MHRA, ANVISHA), and equipment maintenance.
- Quality Control:
- Education: M.Pharm or M.Sc.
- Experience: 2–4 years (Officer/Sr. Officer), 4–6 years (Executive/Sr. Executive).
- Skills: Proficiency in cGMP, GLP, GDP, QMS, AMV, method verification, and regulatory audits.
- Production:
- Operator: ITI with 2–4 years in compression machine operations.
- Officer/Executive: B.Pharm with 2–6 years in production.
- Skills: Knowledge of cGMP, SOPs, BMR/BPR documentation, and regulatory compliance.
- Mandatory: Exposure to EU, MHRA, USFDA, and ANVISHA audits for all roles.
Benefits
- Competitive Salaries:
- Warehouse Manager: INR 8,00,000–12,00,000/year.
- Quality Control: INR 4,00,000–8,00,000/year (based on position and experience).
- Production: INR 3,00,000–7,00,000/year (based on position and experience).
- Career Growth: Opportunities to advance in a leading pharmaceutical company.
- Work Environment: Collaborative, innovative, and focused on quality.
- Regulatory Exposure: Work with global standards (USFDA, EU, MHRA, WHO).
- Health Benefits: Comprehensive wellness programs for employees.
Application Instructions
Attend the walk-in interview on September 16, 2025, from 9:30 AM to 4:30 PM at:
Venue: Plot No. 775, 776 & 628, Vill.: Sakodara, Taluka Bavla, Ahmedabad, Gujarat-382220.
Requirements: Bring your resume and one passport-size photo.
For directions, scan the QR code in the job advertisement or visit Pharmabharat.com.
FAQs
Q: What documents are required for the walk-in interview?
A: Bring a resume highlighting relevant experience and regulatory audit exposure, along with one passport-size photo.
Q: Can candidates apply for multiple roles during the walk-in?
A: Yes, candidates meeting the qualifications for multiple roles can discuss their eligibility with the interview panel.
