Quality Control Senior Associate - Capillary Electrophoresis JP10023
Quality Control Senior Associate - Capillary Electrophoresis JP10023
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Salary Not Disclosed
1 Vacancy
Job Description
Location:West Greenwich RI.
Employment Type: Contract
Business Unit:QC Bioanalytics & Raw Materials Testing
Duration:2 years (with likely extensions and/or conversion to permanent)
Posting Date:3/29/2022
Notes:Candidate will be working on site. Targeting candidates with 46 years of industry/ non academia experience and some Capillary electrophoresis experience
3 Key Consulting is hiring aQuality Control Senior Associatefor a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
Quality Control Separation Sciences lab is searching is for a team member to support testing for routine inprocess and stability samples. This person will be responsible for working in the Quality Control 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 CE (capillary electrophoresis SDSPAGE polysorbate extraction and other general chemistry testing.
- Interacting crossfunctionally 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.
Why is the Position Open
Supplement additional workload on team.
Top Must Have Skills:
- Capillary Electrophoresis experience a must.
- Understanding of quality control and GMP operations.
- Team orientated.
Day to Day Responsibilities:
- Capillary Electrophoresis experience a must.
- Understanding of quality control and GMP operations.
- Team orientated.
Basic Qualifications:
- 46 years of experience in capillary electrophoresis.
- Bachelors Degree in any science field.
- Demonstrated experience in investigations and QC processes.
- Selfmotivated 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 preferably with GMP experience.
- 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 selfmotivated organized able to multitask in timesensitive environments.
Employee Value Proposition:
Great biotech/pharma to work for.
Red Flags:
1. Multiple job movement in short time
2. Mistaking SDSPAGE for CE
Interview process:
Manager interview via Webex
team interview via webex
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this position please feel free to look at the other positions on our websitewww.3keyconsulting/careers. You are welcome to also sharethis opportunity withanyone you think might be interested in applying for this role.
Required Experience:
Senior IC
Employment Type
Full Time
