Sr Manager

BVR People Consulting; Navi Mumbai; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

BVR People Consulting is seeking a senior biotechnology professional in Navi Mumbai to lead the development of downstream processing technologies for biopharmaceutical products, ensuring regulatory compliance. The role requires collaboration with cross-functional teams to design, optimize purification processes for recombinant DNA molecules and to maintain thorough technical documentation.

The ideal candidate will have 15-20 years of experience in the biotech industry with strong knowledge of

Qualifications

• 15-20 years of experience in biotechnology with expertise in downstream processing and purification

Responsibilities

• Lead the development of downstream processing technologies for biopharmaceutical products, ensuring regulatory compliance.
• Collaborate with cross-functional teams to design, optimize, and implement purification processes for recombinant DNA molecules.
• Develop and maintain technical documentation related to downstream processing operations, including protocols, procedures, and reports.
• Provide training and guidance to junior team members on downstream processing techniques and best practices.

Skills

Downstream processing

Chromatography

Filtration

Regulatory compliance

Job description

Roles and Responsibilities :

• Lead the development of downstream processing technologies for biopharmaceutical products, ensuring compliance with regulatory requirements.
• Collaborate with cross-functional teams to design, optimize, and implement purification processes for recombinant DNA molecules.
• Develop and maintain technical documentation related to downstream processing operations, including protocols, procedures, and reports.
• Provide training and guidance to junior team members on downstream processing techniques and best practices.

Job Requirements :

• 15-20 years of experience in biotechnology industry with expertise in downstream processing (e.g., chromatography) and purification (e.g., filtration).
• Strong understanding of regulatory guidelines governing biopharmaceutical manufacturing (e.g., FDA CFR21 Part 600).
• Proven track record of developing successful downstream processing strategies that meet product quality standards.
• Excellent communication skills with ability to work effectively across multiple disciplines.