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Job Requirements of QC Lab Technician I:
-
Employment Type:
Contractor
-
Location:
Belvidere, NJ (Onsite)
Do you meet the requirements for this job?
QC Lab Technician I
Careers Integrated Resources Inc
Belvidere, NJ (Onsite)
Contractor
Job Title: QC Lab Technician I
Job Location: Belvidere, NJ 07823
Job Duration: 11+ Months (Possibility of Extension)
Pay Range: $25/hr. on W2
IMPORTANT: HM is only looking for candidates with 0-3 years of experience for this entry-level role.
Schedule:
Top 3 Skills/Requirements:
Location Details: 100% onsite.
Duration of Project (estimate): 1 year
Potential for Contract to Hire? Yes, *** per hour plus benefits.
Interview Process:mPreferred 1 interview onsite with hiring manager, other supervisor in Quality Department, and manager's supervisor.
Purpose of the Position:
To analyze and/or test under cGMP, raw materials, intermediates and finished products by applying validated or compendia methods.
Position Context:
Position Content:
a) Key areas of accountability/responsibility
Complexity of the Position:
Knowledge and Educational Level:
Required Level of Experience:
Job Location: Belvidere, NJ 07823
Job Duration: 11+ Months (Possibility of Extension)
Pay Range: $25/hr. on W2
IMPORTANT: HM is only looking for candidates with 0-3 years of experience for this entry-level role.
Schedule:
- Confirm Schedule: 8 AM – 4:30 PM Sunday – Thursday
- This will be a Sunday to Thursday first shift schedule.
- During the few weeks/month of training, the analyst will need to report onsite Monday – Friday.
- Once signed off on training, the candidate will begin the Sunday to Thursday schedule.
Top 3 Skills/Requirements:
- Analytical skills.
- Communication/people skills.
- Fits well in team environment.
- Attention to detail.
- Entry level candidates only please.
Location Details: 100% onsite.
Duration of Project (estimate): 1 year
Potential for Contract to Hire? Yes, *** per hour plus benefits.
Interview Process:mPreferred 1 interview onsite with hiring manager, other supervisor in Quality Department, and manager's supervisor.
Purpose of the Position:
To analyze and/or test under cGMP, raw materials, intermediates and finished products by applying validated or compendia methods.
Position Context:
- Performs/Applies knowledge and skills to diverse reactions.
- Release testing of products per current compendia, regulatory and corporate quality systems, and principles.
Position Content:
a) Key areas of accountability/responsibility
- Performs analysis in the laboratory with minimal supervision.
- Prepares standards, mobile phases, and reagents.
- Calibrates and monitors laboratory equipment (HPLC, GC, ICP, etc.).
- Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods.
- Performs calculations, collects and prepares data for evaluation.
- Keeps supervisor informed of work status.
- Investigation of OOS results under guidance of senior staff.
- Maintains good documentation practices.
- Display and promote positive safety behaviors at all times; use proper personal protective equipment, appropriate safety tools, equipment and procedures to ensure that self and others go home safe each day.
- Ensure that area and equipment operate at the highest safety levels.
- Ensure that all people in the area (lab techs, quality personnel, maintenance, visitors, contractors, etc.) comply with the safety directives and keep the area neat and clean.
- Ensure incidents are investigated, reported, and risks are assessed in a timely basis.
- Act in such a way that safety awareness & accident prevention are considered in performing all tasks.
- Show leadership by working to SHEQ standards and encouraging colleagues to work to the same standards.
- All employees to be aware of and follow all Client Life Saving Rules.
- Show leadership by working to support Customer Commitments and encouraging colleagues to work to the same standards.
- Support plant and corporate initiatives as outlined in the manufacturing plan.
- Responsibility for correctness of the determined results.
- Work according to SOP’s and Specification sheets.
Complexity of the Position:
- Demonstrate the ability to learn and perform lab-specific analytical methods.
- Complete analysis on raw materials and finished products within an agreed upon turn around time.
- Ensure SOP’s and specifications are up to date and in compliance with current Compendia and update them if required.
- Perform and document all work associated in adherence with cGMP guidelines.
Knowledge and Educational Level:
- Bachelor’s degree in a relevant Scientific discipline preferred, associate’s degree required.
- Broad/general knowledge of quality control techniques and methods.
- Broad understanding of safety, laboratory hygiene and GMP rules.
- This position is overtime eligible. The schedule may be structured with a required overtime component built-in. Candidates must be able to work shifts, weekends, overtime (including coverage), and holidays as required. All candidates, both internal and external, applying for this position understand that overtime may be required and adjusted based on business needs and to ensure continued safe operations.
Required Level of Experience:
- 0-3 years of lab experience.
- Experience in Microsoft Office (Outlook, Word, and Excel).
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