ROLES & RESPONSIBILITIES

▸ Production Planning & Execution: Implementing production schedules, ensuring timely delivery of products and optimising production processes to improve efficiency and reduce costs; assisting in the setup, operation and monitoring of granulation, compression, coating and packaging machines as per SOPs and batch records; maintaining environmental conditions in the manufacturing area.

▸ Quality Control: Overseeing quality checks throughout the production process; monitoring and controlling process variables that affect product quality.

▸ Documentation: Maintaining accurate, detailed and up-to-date production records including BMRs, BPRs, equipment logs and other relevant documentation; preparing and maintaining master documents (BMR, BPR, PDR, SOP, etc.).

▸ Equipment Management: Ensuring production equipment is properly maintained, routinely cleaned and troubleshooting issues to prevent downtime.

▸ Compliance: Ensuring compliance with current Good Manufacturing Practices (cGMP), safety regulations and other relevant regulatory standards.

▸ Deviation Handling: Investigating deviations, contributing to root cause analysis and CAPA (Corrective and Preventive Action) implementation.

▸ Validation & Qualification: Actively participating in and executing equipment qualification, process validation and revalidation activities.

▸ Coordination: Collaborating with QA, QC and Warehouse departments to ensure smooth and uninterrupted production operations.

▸ Supervision & Training: Supervising, training and guiding production staff on GMP practices, safety & quality standards, company policies and SOP adherence.

▸ Inventory & Continuous Improvement:



Assisting with management of raw materials, packaging materials and consumables inventory; identifying and implementing process improvements to enhance productivity and quality.

ESSENTIAL SKILLS & ATTRIBUTES

✓Technical Knowledge: Sound knowledge of pharmaceutical OSD manufacturing processes, equipment and related technologies including granulation, compression, coating and packaging.

✓ cGMP Knowledge: Knowledge of cGMP, regulatory requirements, quality management systems and documentation control practices.

✓Attention to Detail: Strong attention to detail ensuring accuracy in documentation, in-process quality checks and adherence to SOPs and batch records.

✓Problem-Solving: Ability to identify, analyse and resolve production-related issues including deviations and equipment downtime.

✓Communication & Teamwork: Ability to collaborate effectively with team members and supervisors across departments; smart thinker with mental agility and tactical approach.

✓Organisational Skills: Ability to manage multiple tasks, prioritise effectively and maintain accurate records during simultaneous batch operations.

QUALIFICATIONS

M.Pharm (Pharmaceutics / Pharmacognosy) — Preferred

M.Sc. (Pharmaceutical / Industrial / Applied Chemistry) with 1–2 years of relevant experience

B.Pharm with 1–2 years of relevant experience in OSD pharmaceutical production

Work Experience: 0–2 years in OSD pharmaceutical / nutraceutical manufacturing

Interested candidates can apply through E-mail: [email protected] or whatsapp to (phone hidden)

Pay: ₹270,000.00 - ₹300,000.00 per year

Perks

- Food provided
- Health insurance

Work Location: In person

📌 Junior Executive - Production (Mangalore)
🏢 MEDITEKINDIA
📍 Mangalore