Biotechnologist (Downstream) - Singapore - Amaris Consulting

Amaris Consulting

Verified Company

Singapore

1 week ago

Posted by:

Wei Jie

beBee Recruiter

Description

Who are we? :

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries.

Our solutions focus on four different Business Lines:
Information System & Digital, Telecom, Life Sciences and Engineering.

We're focused on building and nurturing a top talent community where all our team members can achieve their full potential.

Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

Brief Call:
Our process typically begins with a brief virtual/phone conversation to get to know you The objective? Learn about you, understand your motivations, and make sure we have the right job for you

Interviews (the average number of interviews is - the number may vary depending on the level of seniority required for the position).

During the interviews, you will meet people from our team:
your line manager of course, but also other people related to your future role.

We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you.

Of course, you will also get to know Amaris:
our culture, our roots, our teams, and your career opportunities

Case study:
Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.

We look forward to meeting you

Job description:

Amaris will be prioritizing applicants who are currently based in Singapore.

Key Responsibilities:

Operate and maintain downstream bioprocessing equipment, including chromatography systems, viral reduction filtration, ultrafiltration skids, and aseptic filling technologies.
Execute manufacturing activities according to production schedules and in compliance with current Good Manufacturing Practices (cGMP), standard operating procedures, and safety regulations.
Perform inprocess testing and monitoring to ensure product quality and process efficiency.
Collaborate with crossfunctional teams to troubleshoot and resolve processrelated issues.
Participate in process improvement initiatives to enhance manufacturing efficiency and product quality.
Document all manufacturing activities and maintain accurate records in accordance with regulatory requirements.

Qualifications and Skills:

Bachelor's in biotechnology, biochemistry, chemical engineering, or related field.
Experience in downstream biologics manufacturing operations within the biopharmaceutical industry.
Understanding of cGMP regulations and quality systems.
Analytical, problemsolving, and communication skills.
Ability to work effectively in a fastpaced, teamoriented environment