- Location
- West Greenwich, RI
- Workplace
- Onsite
- Type
- Contract
- Department
- Healthcare
- Seniority
- Entry
- Experience
- 1+ years
- Education
- Associate
- Source
- CATS
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.
Job Description:
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)
Overview:
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:
What we are looking for:
Staff augmentation.
Top Must-Have Skill Sets:
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 [email protected]. 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.
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.
Job Description:
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)
Overview:
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
- 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
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.
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 [email protected]. 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.
Skills
GMPCompliance
