Maya Biotech India has announced a walk-in interview drive for experienced pharmaceutical professionals looking to build their careers in sterile and injectable manufacturing. The company is inviting qualified candidates from Quality Control, Quality Assurance, HPLC, GLP, Production, Microbiology, Engineering-QMS, Validation, PPIC, and related departments to attend the recruitment drive.
This hiring initiative offers excellent opportunities for candidates with experience in regulated pharmaceutical manufacturing environments. Professionals seeking career advancement in sterile and injectable facilities can explore multiple openings across various functions.
Walk-In Interview Details
Company Name: Maya Biotech India
Interview Type: Walk-In Interview
Interview Date: 31 May 2026 (Sunday)
Interview Time: 10:00 AM to 04:00 PM
Venue: Hotel MG Regency, NH-21A, Kalka–Baddi Road (Near Traffic Lights), Baddi, Himachal Pradesh, India
Contact Number: +91-8699946046, +91-8209050046
Available Job Openings
Quality Control (QC) – Head/Manager
Experience: 10–15 Years
Vacancies: 1
Quality Assurance (QA) – Manager
Experience: 10–15 Years
Vacancies: 1
HPLC – Officer/Senior Officer
Experience: Up to 4 Years
Vacancies: 8
GLP – Officer/Senior Officer
Experience: Up to 5 Years
Vacancies: 2
QC Raw Material Section – Officer/Senior Officer
Experience: 2–6 Years
Vacancies: 4
QC PM Section – Officer/Senior Officer
Experience: 2–6 Years
Vacancies: 4
Liquid Manufacturing – Manager
Experience: 12+ Years
Vacancies: 2
RM/PM – Senior Executive
Experience: 5–6 Years
Vacancies: 2
RM/PM – Assistant Manager
Experience: 6–10 Years
Vacancies: 2
Engineering-QMS – Executive
Experience: 4–8 Years
Vacancies: 2
QA Validation – Senior Executive
Experience: 5–8 Years
Vacancies: 2
QA-QMS – Senior Executive
Experience: 5–8 Years
Vacancies: 2
Microbiology – Officer/Senior Officer
Experience: 2–4 Years
Vacancies: 3
PPIC – Senior Executive/Assistant Manager
Experience: 7–10 Years
Vacancies: 1
Roles and Responsibilities
• Perform quality control and quality assurance activities as per GMP requirements.
• Handle HPLC analysis, sample testing, calibration, and laboratory documentation.
• Conduct raw material and packaging material testing.
• Support sterile and injectable manufacturing operations.
• Execute process validation, equipment validation, and cleaning validation activities.
• Manage environmental monitoring, sterility testing, and microbiological analysis.
• Maintain QMS documentation, SOPs, audit compliance, and regulatory requirements.
• Coordinate production planning and inventory management activities in PPIC functions.
Required Qualifications
• B.Pharm, M.Pharm, B.Sc, M.Sc, B.Tech, M.Tech, or other relevant life sciences qualifications.
• Relevant experience in pharmaceutical manufacturing, especially sterile or injectable facilities.
• Knowledge of GMP, GLP, QMS, validation, documentation, audits, and regulatory compliance.
• Strong communication and technical skills.
Salary and Benefits
Selected candidates can expect competitive salary packages based on qualifications, experience, and current compensation. Additional benefits may include:
• Performance-based growth opportunities
• Exposure to regulated pharmaceutical manufacturing
• Professional development and training
• Career advancement opportunities
• Employee-friendly work environment
Documents Required
Candidates attending the interview should carry:
• Updated Resume/CV
• Educational Certificates
• Experience Certificates
• Current CTC Details
• Recent Salary Slips (if applicable)
• Government Identity Proof
How to Apply
Interested and eligible candidates can directly attend the walk-in interview on 31 May 2026 at the specified venue. Candidates are advised to reach the venue on time and carry all required documents for a smooth interview process.
