At Steribio Lifesciences, we dont just manufacture IV fluids we deliver lifelines. Born from a vision to transform patient care, our story is rooted in passion, precision, and purpose.

Because at Steribio, every drop saves a life and every life deserves the best.

Position: QA Manager

Location: Patas

Experience: 8 to 10 years

Industry: Pharmaceutical (LVP formulations Injectables)

Roles & Responsibilities

Quality Policies and Procedures:

Quality Standards:

Regulatory Compliance:

Quality Audits:

Quality Control:

Process Improvement:

Root Cause Analysis:

Documentation:

Training and Education:

Preferred candidate profile

Key Skills & Competencies:

Strong knowledge of cGMP, WHO, , and other regulatory standards.

Hands-on experience in Injectables manufacturing.

Expertise in equipment qualification, FAT/SAT, validation, and vendor audits.

Strong analytical skills to assess quality risks and implement proactive solutions.

Excellent documentation, communication, and leadership abilities.

Ability to work in a start-up manufacturing environment and build systems from the ground up.

Qualifications & Experience:

B.Pharm / M.Pharm / M.Sc. in Pharmaceutical Sciences or related field.
10+ years of experience

in

Quality Assurance (QA)

in a

pharmaceutical manufacturing setup.
Must have experience in handling LVP Injectable dosage forms.
Experience in setting up

QA systems for new manufacturing facilities

will be highly preferred.

More Jobs at Steribio

Manager - Quality Assurance (QA) - Formulation Injectables

pune

8.0 - 10.0 yrs

INR 0 - 1 Lacs

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