Job Description

Job Title: Associate Quality Control, Biopharma (JP100171)
Location: West Greenwich, RI.
Employment Type: Contract
Business Unit: Quality Control, Bio-Analytics, and Raw Materials Testing
Duration: 2 years with likely extension or conversion to FTE
Posting Date: 5/5/2022
Notes: 100% onsite

3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.

Experience with LIMS would be a great preference - analytical data reporting system
Compendia experience is a plus but not required
Lab experience is a must (pro or academia)

Quality Control is searching is for an analyst to support routine testing of Raw Materials.
This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.

The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.

Responsibilities will include, but are not limited to:

Performing analytical testing for general chemistry (pH, osmolality, appearance, etc.),
Interacting cross-functionally with a wide variety of people and teams;
Troubleshoot, solve problems and communicate with stakeholders.
Participate in initiatives and projects that may be departmental or organizational in scope.
Evaluate lab practices for compliance and operational excellence on a continuous basis.

What we are looking for:

Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.
Demonstrated ability to work independently and deliver right first time results
Excellent communication skills (written and verbal)
Must have focus on data integrity
Qualified to work in the U.S. without employer sponsorship
Commitment of a 40-hour work week in West Greenwich, RI
Experience: Bachelor’s degree OR Associate's degree and 1-2 years of Quality or Analytical Laboratory experience

Preferred Qualifications:

1-3 years of experience in GMP analytical laboratory
Experience with bench chemistry
Experience with Compendial testing
Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision
Strong communication skills (both written and oral), facilitation and presentation skills
Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.
Understanding of biopharmaceuticals process and related unit operations
Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy
Independent, self-motivated, organized, able to multi-task in time-sensitive environments.
Demonstrated experience in investigations and QC processes

Why is the Position Open?
Staff augmentation.

Top Must-Have Skill Sets:

Strong Analytical Skills
Must have lab experience - (pro or academia)
Bachelor’s degree/Associates or Highschool degree with 1-3 years of experience in GMP analytical laboratory
Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.
Interpersonal Skills: Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to participate in lean initiatives on site.

Day to Day Responsibilities:
Daily responsibilities will be focused on executing analytical testing of raw materials in a GMP laboratory.

Basic Qualifications:
Quality control lab experience and use of HPLC/UPLC equipment is preferred

Red Flags:
Candidates with no prior lab experience

Interview process:
Phone screening of possible candidates. Possible second phone screen and/or in-person interview for those who pass the initial phone screening.

We invite qualified candidates to send your resume to recruiting@3keyconsulting.com If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.

About 3 Key Consulting, Inc.

3Key Consulting specializes in the rapid recruitment and placement of business and IT professional within the life sciences and healthcare industries. With 12 years of experience, 3Key has established a vast network of industry professionals and forged strong partnerships/alliances with key academic institutions across the country to continually develop our business professional and niche skill pipeline.

3KC offers a full suite of staffing solutions including PEO and compliance services. 3KC has several technology and industry domain practices including competencies in business intelligence, healthcare and life sciences.

People, process, and technology are 3 key areas of focus that we carefully examine individually and jointly, in order to deliver on our client's 3 key areas of focus - better, faster and cost effective BI and staffing solutions.

MISSION:

To create a better work experience for our customers, partners and employees through exceptional dedication and performance.

• We make hiring easier

• We build strong teams

• We bring about positive outcomes

VISION:

3 Key Consulting’s responsibility is to continually improve the manner and efficiency in which human resources and businesses are brought together to create value. Our vision is to put programs into action that improve market efficiencies while helping businesses and people be more productive.

Industry

Unknown

Company Size

1-10 employees

Headquarters

Simi Valley, CA

Year Founded

2009

Website

3keyconsulting.com

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