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Opes Healthcare Mega Walk-in Interview Drive – Multiple Positions in Regulatory Affairs, Production, QA, F&D, ADL, Warehouse & More on 29th March 2026

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Pharma Jobs – Opes Healthcare is conducting a mega walk-in interview on 29th March 2026 for experienced professionals in Regulatory Affairs, TPO Sterile Operations, Production Planning, Quality Assurance, Formulation Development, Analytical Development, Warehouse, Purchase, PPMC, Packaging Development, and Microbiology roles.

This is a major hiring opportunity for candidates with pharma formulation experience seeking regulatory affairs jobs, production jobs, QA jobs, F&D jobs, ADL jobs, and pharma careers in Ahmedabad/Gujarat.

About the Company

Opes Healthcare is a dynamic pharmaceutical organization specializing in third-party operations (TPO), sterile injectables, ophthalmic products, and formulations for semi-regulated and regulated markets.

With a focus on quality, compliance, and timely delivery, the company supports global pharmaceutical partners through end-to-end manufacturing, development, and regulatory services.

Opes maintains high standards of GMP, validation, and documentation, offering a professional environment for growth in formulation development, quality systems, and sterile operations.

Job Details

  • Company Name: Opes Healthcare
  • Experience: Varies by role (1–12 years)
  • Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc / Diploma in Packaging Technology
  • Location: Ahmedabad, Gujarat (corporate / operational base)
  • Work Type: On-site

Job Description

Opes Healthcare is expanding its third-party sterile operations, formulation development, quality, and support functions. The mega walk-in invites candidates with hands-on experience in regulated pharma environments to support injectable/ophthalmic manufacturing, regulatory submissions, quality assurance, and analytical activities.

Regulatory Affairs – Executive to Sr. Executive / Manager

  • Department: Regulatory Affairs
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Executive to Sr. Executive / Manager
  • Experience: Executive: 5–7 Years | Manager: 10–12 Years
  • Education/Qualification: B.Pharm / M.Pharm

TPO Sterile (Third Party Operation) – Production Management & Operations

  • Department: Production (TPO Sterile)
  • Market: Pharmaceuticals – Sterile Injectables & Ophthalmics
  • Role: Various (Officer to Manager level)
  • Experience: Officer: 3–5 Years | Manager: 10–12 Years
  • Education/Qualification: B.Pharm / M.Pharm

Quality Assurance – Officer to Sr. Executive

  • Department: Quality Assurance
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Officer to Sr. Executive – QA
  • Experience: 2–6 Years
  • Education/Qualification: B.Pharm / M.Pharm

Formulation Development (F&D) – Sterile – Officer to Executive

  • Department: Formulation Development (F&D) – Sterile
  • Market: Pharmaceuticals – Sterile Injectables & Ophthalmics
  • Role: Officer to Executive – F&D
  • Experience: 1–4 Years
  • Education/Qualification: B.Pharm / M.Pharm

Analytical Development Laboratory (ADL) – Officer to Executive

  • Department: Analytical Development Laboratory (ADL)
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Officer to Executive – ADL
  • Experience: 1–4 Years
  • Education/Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm

Warehouse (Store) – Officer to Executive

  • Department: Warehouse / Stores
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Officer to Executive – Warehouse
  • Experience: 1–5 Years
  • Education/Qualification: Any Graduate

Purchase – Officer to Executive

  • Department: Purchase
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Officer to Executive – Purchase
  • Experience: 6 Months–5 Years
  • Education/Qualification: Any Graduate

PPMC – Officer to Sr. Officer

  • Department: Production Planning & Material Control (PPMC)
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Officer to Sr. Officer – PPMC
  • Experience: 1–3 Years
  • Education/Qualification: Any Graduate

Packaging Development Cell (PDC) – Sr. Executive

  • Department: Packaging Development Cell (PDC)
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Sr. Executive – PDC
  • Experience: 5–7 Years
  • Education/Qualification: B.Sc / M.Sc / B.Pharm / D.Pharm / Diploma in Packaging Technology

Microbiology – Executive to Sr. Executive (Only Female)

  • Department: Quality Control – Microbiology
  • Market: Pharmaceuticals – Sterile & Ophthalmic Formulations
  • Role: Executive to Sr. Executive – Microbiology
  • Experience: 5–7 Years
  • Education/Qualification: B.Sc / M.Sc (Microbiology)

Skills/Qualifications

  • Formulation background in sterile injectables/ophthalmics mandatory
  • Expertise in dossier preparation, global submissions (CIS & LATAM markets)
  • Hands-on experience in IPQA, validation, QMS, CAPA, deviation handling
  • Proficiency in analytical method development, validation, stability studies
  • Knowledge of RM/PM material management, dispensing, and inventory control
  • Strong documentation, regulatory compliance, and audit readiness skills

Key Responsibilities

  • Manage regulatory dossier preparation and global submissions
  • Oversee TPO sterile operations, manufacturing, and process improvement
  • Perform IPQA checks, validation, and QMS activities
  • Develop and validate analytical methods for sterile products
  • Handle RM/PM receipt, dispensing, storage, and inventory
  • Support production planning, material control, and packaging development
  • Conduct microbial testing, environmental monitoring, and OOS/OOT investigations

Benefits/Perks

  • Career growth in a fast-growing sterile pharma organization
  • Exposure to regulated markets and third-party operations
  • Opportunities for skill development in QMS, validation, and microbiology
  • Competitive compensation and attractive HR policies
  • Supportive work culture with focus on quality and employee well-being
  • AC transportation facility available

How to Apply

Walk-in interview is open on 29th March 2026 from 09:30 AM to 03:00 PM. Bring updated CV, salary slips for the last three months, and relevant documents.

Opes Healthcare Mega Walk-in Interview Drive – Multiple Positions in Regulatory Affairs, Production, QA, F&D, ADL, Warehouse & More on 29th March 2026

Candidates unable to attend can email CV to career@opeshealthcare.com. For more sterile pharma jobs, QA/QC openings, production roles, and walk-in interviews in Gujarat, visit Pharma Recruiter.

Walk in on 29th March 2026 and join Opes Healthcare’s growing team!

Walk-in Interview Details

  • Date: 29th March 2026
  • Time: 09:30 AM – 03:00 PM
  • Venue: 411 and 412, Block-A, Navratna Corporate Park, Ambli Rd, Ashok Vatika, Ahmedabad, Gujarat – 380058
  • Contact: 85118 49377 | 74868 29377 | career@opeshealthcare.com

Why You Should Join

Opes Healthcare provides a dynamic, quality-focused environment in the sterile injectables and ophthalmic segment with a strong emphasis on third-party operations and regulated markets.

Employees benefit from hands-on experience in formulation development, validation, QMS, and microbiology, career advancement from officer to managerial levels, attractive HR policies, and long-term stability in Gujarat’s pharmaceutical ecosystem.

Joining Opes means contributing to high-quality, compliant products while growing professionally in a supportive, growth-driven organization.

FAQs

What experience is required for Regulatory Affairs roles at Opes Healthcare?

Executive: 5–7 years; Manager: 10–12 years with expertise in dossier preparation and global submissions (CIS & LATAM markets).

Are freshers eligible for any positions?

No—the current openings require 1+ years experience; focus is on regulated sterile/ophthalmic formulation background.

Where is the walk-in venue located?

411 and 412, Block-A, Navratna Corporate Park, Ambli Rd, Ashok Vatika, Ahmedabad – 380058, Gujarat.

What growth opportunities exist at Opes Healthcare?

Strong potential for career progression in a fast-growing sterile pharma company with exposure to TPO operations, validation, QMS, and regulated market submissions.

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