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Form of work Position Details:
Our client, a world-leading Pharmaceutical Company in Sanford, NC is currently looking for a QC Chemist to join their expanding team.
Job Title: QC Chemist / Pharma Industry
Duration: 4 months contract, extendable up to 36 Months
Location: Sanford, NC
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Position Summary:
The position will support the Pharmaceutical Sanford, NC Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, validation, and stability.
Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; testing; analyzing, interpreting, and trending results; and creating, reviewing and approving documentation.
At a minimum, the individual should be considered able to demonstrate the following:
acts safely and follows all EH&S safety requirements for site and QC laboratories
sufficient depth of knowledge within their scientific discipline and previous area of experience
good written and verbal communication techniques
ability to follow written procedures and learn from hands on training
capability of solving complex mathematical and situation dependent problems
ability to receive feedback and take accountability for actions and personal development
aptitude for good decision making based on procedures, guidance, and experience
awareness to know their own limitations and seek senior scientist or management guidance when appropriate
desire to ensure correctness and accuracy in tasks and documentation, detail oriented
fitness of functioning as a team member and performing independent work with minor guidance
willingness to use personal skills and knowledge to achieve individual and company goals and objectives
Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft OfficeTM applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs.
Position Responsibilities:
Responsible for knowing, understanding and acting in accordance with Pharmaceutical's values and our OWNIT culture.
Performs tasks associated with maintaining GMP compliant Quality Control and Stability laboratories.
Performs lab support duties including, but not limited to ordering and stocking consumables, reagent receipt and disposal, laboratory and equipment cleanings and other general support duties.
Use of general laboratory equipment (i.e. balance, pH meter, glass washer, autoclave etc.)
Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.) and ensuring adherence to Pharmaceutical standards, guidelines and values.
Responsible for reporting issues to management and participating in issue resolution (such as reporting OOS result and participating in associated laboratory investigation, reporting instrument issues and assisting with troubleshooting, etc.)
Assessing existing situations and suggesting improvements to increase compliance and innovation.
Organizational Relationships:
The Quality Control Chemistry group, micro group, and lab support group.
Education And Experience:
0 - 3 years of manufacturing, quality or analytical testing experience in the biotech or pharmaceutical industry.
BS/BA Degree in Science/related field with experience in biotech or pharmaceutical industry is preferred; however, other appropriate combinations of education and/or experience in the biotech or pharmaceutical industry are suitable.
Understanding of laboratory practices and analytical testing and use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity, and various other instruments.
Technical Skills Requirements:
Computer skills.
Understanding of laboratory practices and analytical testing and use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity, and various other instruments.
Physical Position Requirements:
Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.
Required Skills:
Problem solving
good communication skills
good team player
Preferred Skills:
GMP
Lab Experience
Day 2 Day Functions:
Washing glassware, stocking, ordering lab supplies, stocking/inventorying, and disposing of waste.
Interview Preference:
Teams
Comments:
100% on-site (Will need to adhere to return to site policy)
Assignment duration: 4-months
Interview Process:
possible panel
Minimum Education:
High School
Associate Degree/ BA acceptable
Our client, a world-leading Pharmaceutical Company in Sanford, NC is currently looking for a QC Chemist to join their expanding team.
Job Title: QC Chemist / Pharma Industry
Duration: 4 months contract, extendable up to 36 Months
Location: Sanford, NC
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Position Summary:
The position will support the Pharmaceutical Sanford, NC Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, validation, and stability.
Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; testing; analyzing, interpreting, and trending results; and creating, reviewing and approving documentation.
At a minimum, the individual should be considered able to demonstrate the following:
acts safely and follows all EH&S safety requirements for site and QC laboratories
sufficient depth of knowledge within their scientific discipline and previous area of experience
good written and verbal communication techniques
ability to follow written procedures and learn from hands on training
capability of solving complex mathematical and situation dependent problems
ability to receive feedback and take accountability for actions and personal development
aptitude for good decision making based on procedures, guidance, and experience
awareness to know their own limitations and seek senior scientist or management guidance when appropriate
desire to ensure correctness and accuracy in tasks and documentation, detail oriented
fitness of functioning as a team member and performing independent work with minor guidance
willingness to use personal skills and knowledge to achieve individual and company goals and objectives
Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft OfficeTM applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs.
Position Responsibilities:
Responsible for knowing, understanding and acting in accordance with Pharmaceutical's values and our OWNIT culture.
Performs tasks associated with maintaining GMP compliant Quality Control and Stability laboratories.
Performs lab support duties including, but not limited to ordering and stocking consumables, reagent receipt and disposal, laboratory and equipment cleanings and other general support duties.
Use of general laboratory equipment (i.e. balance, pH meter, glass washer, autoclave etc.)
Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.) and ensuring adherence to Pharmaceutical standards, guidelines and values.
Responsible for reporting issues to management and participating in issue resolution (such as reporting OOS result and participating in associated laboratory investigation, reporting instrument issues and assisting with troubleshooting, etc.)
Assessing existing situations and suggesting improvements to increase compliance and innovation.
Organizational Relationships:
The Quality Control Chemistry group, micro group, and lab support group.
Education And Experience:
0 - 3 years of manufacturing, quality or analytical testing experience in the biotech or pharmaceutical industry.
BS/BA Degree in Science/related field with experience in biotech or pharmaceutical industry is preferred; however, other appropriate combinations of education and/or experience in the biotech or pharmaceutical industry are suitable.
Understanding of laboratory practices and analytical testing and use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity, and various other instruments.
Technical Skills Requirements:
Computer skills.
Understanding of laboratory practices and analytical testing and use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity, and various other instruments.
Physical Position Requirements:
Ability to lift 30 lbs, stand for 2 to 3 hours at a time, sit for 2 to 3 hours at a time, walk long distances and bend to obtain items from lower shelving/cabinets.
Required Skills:
Problem solving
good communication skills
good team player
Preferred Skills:
GMP
Lab Experience
Day 2 Day Functions:
Washing glassware, stocking, ordering lab supplies, stocking/inventorying, and disposing of waste.
Interview Preference:
Teams
Comments:
100% on-site (Will need to adhere to return to site policy)
Assignment duration: 4-months
Interview Process:
possible panel
Minimum Education:
High School
Associate Degree/ BA acceptable
