Vencora Healthcare Pvt. Ltd. has announced exciting career opportunities for experienced pharmaceutical professionals. The company is inviting applications for Quality Assurance Manager/Assistant Manager and Formulation & Development Executive positions. Candidates with relevant experience in Quality Assurance, Product Development, Documentation, and Manufacturing Support are encouraged to apply.

If you are looking to build a rewarding career in the pharmaceutical manufacturing industry, this is an excellent opportunity to join a fast-growing organization focused on quality, innovation, and excellence.

About Vencora Healthcare Pvt. Ltd.

Vencora Healthcare Pvt. Ltd. is a rapidly growing pharmaceutical manufacturing company committed to delivering high-quality healthcare solutions. The company emphasizes innovation, compliance with international quality standards, and continuous professional development.

Company Motto: Better Health. Better Tomorrow.

Job Details

Particular Details

Company Name

Vencora Healthcare Pvt. Ltd.

Industry

Pharmaceutical Manufacturing

Job Type

Full-Time

Experience Required

2–8 Years

Selection Process

Resume Shortlisting, Technical Interview & HR Interview

Application Mode

Email / Contact HR

Open Positions

1. Quality Assurance Manager / Assistant Manager

Experience

5–8 Years

Key Responsibilities

Oversee Quality Assurance Systems.

Handle GMP documentation and compliance.

Conduct internal audits.

Lead QA operations.

Team management and training.

Ensure regulatory compliance.

Vacancies: 1

2. Formulation & Development Executive

Experience

2–5 Years

Key Responsibilities

Product formulation and development.

Manufacturing process support.

Batch monitoring and documentation.

Coordination between Production and R&D.

Process optimization and validation support.

Vacancies: 1

Why Join Vencora Healthcare?

Excellent career growth opportunities.

Professional and supportive work culture.

Exposure to advanced pharmaceutical manufacturing standards.

Opportunity to work with an innovative and dynamic team.

Focus on quality, innovation, and employee development.

Skills Required

Good Manufacturing Practices (GMP)

Good Documentation Practices (GDP)

Pharmaceutical Quality Assurance

Documentation Management

Product Formulation

Process Validation

Regulatory Compliance

Internal Auditing

CAPA & Change Control

Teamwork and Communication Skills

Educational Qualification

Candidates should possess qualifications relevant to pharmaceutical manufacturing, such as:

B.Pharm

M.Pharm

M.Sc.

Other relevant Life Science qualifications

(Qualification should match the job profile and experience.)

Selection Process

The recruitment process generally includes:

Resume Screening

Technical Interview

HR Interview

Final Selection

Offer Letter

How to Apply

Interested and eligible candidates can send their updated resume or contact the HR team using the details below.

Email: vencorahealthcare@gmail.com

Contact Numbers:

+91 99798 87581

+91 97266 63332

Website: www.vencorahealthcare.com

Documents Required

Updated Resume

Educational Certificates

Experience Certificates

Latest Salary Slip (if applicable)

Government Photo ID

Passport-size Photograph

Important Note

Candidates should carefully verify all eligibility criteria before applying. Carry original documents during the interview process if requested by the company. Applications from candidates with relevant pharmaceutical manufacturing experience will be given preference.

Technical FAQs

1. What is the primary responsibility of a Quality Assurance Manager in a pharmaceutical company?

A Quality Assurance Manager ensures that manufacturing processes comply with GMP guidelines, regulatory requirements, and internal quality standards. They oversee documentation, audits, deviations, CAPA, change control, and quality systems.

2. What does a Formulation & Development Executive do?

A Formulation & Development Executive develops new pharmaceutical formulations, optimizes manufacturing processes, performs stability studies, supports technology transfer, and coordinates with Production and Quality departments.

3. What GMP knowledge is expected for these roles?

Candidates should understand Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), SOP preparation, batch manufacturing records, deviation handling, CAPA, change control, validation, and regulatory compliance.

4. Which pharmaceutical documents should experienced candidates be familiar with?

Professionals should have knowledge of Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), Standard Operating Procedures (SOPs), Specifications, Validation Protocols, Calibration Records, and Quality Management System (QMS) documentation.

5. Which technical skills improve selection chances?

Strong knowledge of pharmaceutical manufacturing, GMP compliance, documentation practices, audit handling, process validation, formulation development, analytical thinking, problem-solving, and effective communication significantly enhance a candidate’s chances of selection.