Stivaph Hiring B.Pharm, M.Pharm, MBA, CA

Stivaph Hiring B.Pharm, M.Pharm, MBA, CA

B.Pharm, M.Pharm 20+ Vacancies Ahmedabad

B.Pharm, M.Pharm, MBA, CA hiring for 20+ pharma vacancies in Ahmedabad at Stivaph Healthcare Pvt. Ltd.

Stivaph Healthcare Pvt. Ltd. is expanding its pharmaceutical operations and inviting applications from experienced pharma professionals across multiple departments including Production, Quality Assurance, Quality Control, Regulatory Affairs, Engineering, Warehouse, Purchase, Business Development, HR, and Administration. This large-scale hiring drive is focused strictly on candidates with pharmaceutical industry experience, particularly those with exposure to GMP-compliant manufacturing environments.

If you are searching for pharma jobs in Ahmedabad, regulatory affairs careers in Gujarat, production manager roles in formulation plants, or quality control officer openings in a growing pharmaceutical company, this opportunity deserves attention.

Company Overview

Stivaph Healthcare Pvt. Ltd. operates from Sanand GIDC II, Ahmedabad, one of Gujarat’s rapidly developing pharmaceutical manufacturing zones. The company focuses on formulation development and commercial manufacturing, including liquid and ointment dosage forms.

With a structured plant setup and corporate office in Ahmedabad, Stivaph follows GMP guidelines and regulated documentation systems. The organization emphasizes quality compliance, validated processes, and cross-functional coordination across production, QA, QC, warehouse, and regulatory departments.

As the pharmaceutical sector continues to expand in regulated and semi-regulated markets, companies like Stivaph play a direct role in strengthening India’s formulation manufacturing capacity. Professionals joining the company gain exposure to pharmaceutical compliance systems, regulatory documentation, validation processes, and supply chain management — all critical for long-term career growth in life sciences.

Job Role & Responsibilities

Stivaph Healthcare is hiring across the following departments:

Production Department (Solid, Liquid & Ointment)

Designations: Operator, Officer, Executive, Manager

Experience Range: 1–10 Years

Key Responsibilities:

  • Handling compression, coating, granulation, and capsule filling operations
  • Managing liquid and ointment production lines
  • Ensuring batch manufacturing record (BMR) compliance
  • Supervising machine operators and shift activities
  • Maintaining cGMP documentation and line clearance procedures
  • Coordinating with QA for in-process quality checks

Machine Operators (ITI qualified) must have exposure to compression, granulation, and capsule filling equipment.

Quality Assurance (QA)

Designations: Executive, Sr. Executive, Manager

Experience: 3–10 Years

Key Responsibilities:

  • Managing Quality Management Systems (QMS)
  • Handling deviations, CAPA, change control
  • Conducting internal audits and compliance reviews
  • Batch record review and release documentation
  • Supporting regulatory inspections and audit preparedness

QA professionals contribute directly to regulatory compliance and pharmaceutical quality systems integrity.

Quality Control (QC)

Designations: Officer, Executive, Sr. Executive

Experience: 1–4 Years

Key Responsibilities:

  • Raw material and finished product testing
  • Analytical Method Validation (AMV)
  • Handling HPLC, UV, and other analytical instruments
  • Stability studies and documentation
  • OOS/OOT investigations

Quality Control – Microbiology

Designation: Officer

Experience: 1–3 Years

Responsibilities:

  • Environmental Monitoring (EM)
  • Microbial testing and culture handling
  • Water system monitoring
  • Sterility and contamination control documentation

Regulatory Affairs

Designation: Officer / Executive / Assistant Manager / Manager

Qualification: M.Pharm

Experience: 3–8 Years

Responsibilities:

  • Dossier preparation (CTD/eCTD)
  • Product registration documentation
  • Regulatory submission coordination
  • Variation filing and lifecycle management

Regulatory Affairs remains one of the highest growth and high CPC domains within the pharmaceutical sector.

Purchase Department

Designation: Sr. Executive / Assistant Manager

Qualification: B.Pharm

Experience: 3–6 Years

Responsibilities:

  • Vendor management
  • Raw material procurement
  • Cost negotiation and compliance documentation

Business Development

Designation: Executive / Head / General Manager / Vice President

Qualification: Science Graduate / MBA

Experience: 2–25 Years (Based on role)

Responsibilities:

  • Market expansion strategy
  • Contract manufacturing acquisition
  • Client relationship management
  • Revenue growth planning

Engineering Department

Designation: Engineer / Plant Supervisor / Senior Manager

Qualification: Electrical Diploma / Engineering Degree

Experience: 3–12 Years

Responsibilities:

  • Preventive maintenance
  • Utility and HVAC management
  • Equipment qualification support
  • Plant supervision and infrastructure reliability

Warehouse

Designation: Officer / Manager

Qualification: Any Graduate

Experience: 1–9 Years

Responsibilities:

  • Inventory control
  • Material inward and outward documentation
  • GMP storage compliance
  • Coordination with production and QA

Human Resources & Administration

Qualification: MBA / MHRM / Any Graduate

Experience: 2–5 Years

Responsibilities:

  • Recruitment coordination
  • Payroll and employee documentation
  • Compliance with labor regulations
  • Administrative operations

Chartered Accountant (CA)

Qualification: CA Cleared

Designation: Manager

Experience: 5–9 Years

Responsibilities:

  • Financial compliance
  • Audit handling
  • Budget planning and cost control

Eligibility / Qualifications

Relevant educational backgrounds include:

B.Pharm, M.Pharm, B.Sc., M.Sc., MBA, MHRM, Chartered Accountant (CA), ITI, Diploma (Electrical), Engineering Degree, Science Graduate, Any Graduate (with pharma experience).

Relevant courses include: Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy, Regulatory Affairs, Analytical Chemistry, Microbiology, Biotechnology, Life Sciences, Finance, Human Resource Management, Mechanical Engineering, Electrical Engineering.

Important Note: Only candidates with pharmaceutical industry experience are eligible to apply.

Freshers from B.Pharm and M.Pharm backgrounds may apply for selected entry-level roles.

Location & Work Details

Plant Address:
Sanand GIDC II, Village Bol, Taluka Sanand, District Ahmedabad, Gujarat – 382170

Corporate Office:
6th Floor, Tipsons House, Dr. Vikram Sarabhai Marg, Opp. The Project Café, Ambawadi, Ahmedabad

Stivaph’s location in Sanand GIDC provides proximity to major pharma clusters and logistics networks, offering strong career stability in Gujarat’s pharmaceutical manufacturing ecosystem.

Salary will be aligned with experience, designation level, and industry standards.

Application Process

Interested candidates can share their updated resume at:

hr@stivaph.com
Contact: +91-92130 15700
Website: www.stivaph.com

Ensure your resume clearly mentions:

  • Department applied for
  • Total pharma experience
  • Current CTC and expected CTC
  • Notice period

Shortlisted candidates will be contacted for further technical and HR discussions.

Why Join Stivaph Healthcare?

  • Multi-department career growth opportunities
  • Exposure to regulated pharmaceutical manufacturing
  • Structured GMP and quality systems
  • Leadership openings up to Vice President level
  • Strong presence in Gujarat pharma manufacturing hub

Professionals seeking pharmaceutical production jobs in Ahmedabad, QA manager openings, QC analytical method validation careers, regulatory affairs manager roles, or pharma business development leadership positions should evaluate this opportunity seriously.

Frequently Asked Questions (FAQs)

1. Is pharma experience mandatory?

Yes. Only candidates with pharmaceutical industry experience are eligible.

2. Can freshers apply?

Freshers from B.Pharm and M.Pharm can apply for select entry-level roles.

3. Are multiple senior-level roles available?

Yes. Positions range from Operator and Officer to Senior Manager and Vice President levels.

4. How to apply?

Send your resume to hr@stivaph.com or contact +91-92130 15700.

5. Is this a plant-based role?

Yes. Most roles are based at the Sanand GIDC II manufacturing plant.


Job Summary Table

Company Stivaph Healthcare Pvt. Ltd.
Vacancies Production Operator, QA Executive, QC Officer (AMV), QC Micro Officer, Regulatory Affairs Manager, Purchase Executive, Business Development Executive/VP, Engineering Supervisor, Warehouse Officer/Manager, HR Executive, Chartered Accountant
Required Education B.Pharm, M.Pharm, B.Sc., M.Sc., MBA, MHRM, CA, ITI, Diploma, Engineering Degree, Any Graduate (Pharma Experience)
Experience 1–25 Years (Role Dependent)
Stivaph Hiring B.Pharm, M.Pharm, MBA, CA
Stivaph Hiring B.Pharm, M.Pharm, MBA, CA

To apply for this job email your details to hr@stivaph.com


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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