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Urgent Opening Qc Lab Technician Hour

  • ... Posted on: Oct 02, 2024
  • ... Select Source International
  • ... Belvidere, New Jersey
  • ... Salary: Not Available
  • ... Full-time

Urgent Opening Qc Lab Technician Hour   

Job Title :

Urgent Opening Qc Lab Technician Hour

Job Type :

Full-time

Job Location :

Belvidere New Jersey United States

Remote :

No

Jobcon Logo Job Description :

My name is Gabriel, and I am a Recruitment Professional with Select Source International, a global staffing agency.

I am reaching out today because I came across your resume on Monster, and I believe your experience and skill set would make you an ideal candidate for a QC Lab Technician 1 role that I am looking to fill in Belvidere NJ 07823.

Please review the job description I have provided below and, if you are interested, reach out to me at: (612) 474-9548. I am available anytime from 8:30 am 5:30 pm CST. You may also reply to this email by providing me with the best contact number and time frame for me to give you a call.

These positions do move fast, so time is of the essence. I look forward to hearing from you soon!

Job Title: QC Lab Technician 1

Payrate: $25/Hour on w2

Location: 206 Macks Island Drive, Belvidere NJ 07823

Duration: 12+ months

Shift: 8AM - 4:30 PM Tues - Sat

Description:

Top 3 Skills/Requirements: Analytical skills, communication/people skills, fits well in team environment, attention to detail

Interview Process: preferred 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 -

1. Performs/Applies knowledge and skills to diverse reactions.

2. Release testing of products per current compendia, regulatory and corporate quality systems, and principles.

Position content-

a) Key areas of accountability/responsibility

1. Performs analysis in the laboratory with minimal supervision.

2. Prepares standards, mobile phases, and reagents.

3. Calibrates and monitors laboratory equipment (HPLC, GC, ICP, etc.)

4. Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods.

5. Performs calculations, collects and prepares data for evaluation.

6. Keeps supervisor informed of work status

7. Investigation of OOS results under guidance of senior staff

8. Maintains good documentation practices. SHE Duties & Responsibilities: 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; that area and equipment operate at the highest safety levels; 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.

9. Ensures incidents are investigated, reported, and risks are assessed in a timely basis.

10. Acts in such a way that safety awareness & accident prevention are considered in performing all tasks

11. Shows leadership by working to SHEQ standards and encouraging colleagues to work to the same standards.

12. All employees to be aware of and follow all DSM Life Saving Rules.

13. Shows leadership by working to support Customer Commitments and encouraging colleagues to work to the same standards.

14. Supports plant and corporate initiatives as outlined in the manufacturing plan.

a) Projects/special assignments

1. Responsibility for correctness of the determined results.

2. Work according to SOP's and Specification sheets.

Complexity of the position-

1. Demonstrate the ability to learn and perform lab specific analytical methods

2. Complete analysis on raw materials and finished products within an agreed upon turnaround time.

3. Ensures SOP's and specifications are up to date and in compliance with current Compendia and updates them if required.

4. Performs and documents all work associated in adherence with cGMP guidelines.

Knowledge and educational level -

1. Bachelor's degree in a relevant Scientific discipline preferred, associate's degree required.

2. Broad / General knowledge of quality control techniques and methods.

3. Broad understanding of safety, laboratory hygiene and GMP rules

4. 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 experiences -

1. 0-3 years of lab experience

2. Experience in Microsoft Office (outlook, word, and excel)

Jobcon Logo Position Details

Posted:

Oct 02, 2024

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-bfe4684908234e4747db49fdf44e49e96ba8a6ebf03e4b60de17ea79fc62b912

City:

Belvidere

Job Origin:

CIEPAL_ORGANIC_FEED

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My name is Gabriel, and I am a Recruitment Professional with Select Source International, a global staffing agency.

I am reaching out today because I came across your resume on Monster, and I believe your experience and skill set would make you an ideal candidate for a QC Lab Technician 1 role that I am looking to fill in Belvidere NJ 07823.

Please review the job description I have provided below and, if you are interested, reach out to me at: (612) 474-9548. I am available anytime from 8:30 am 5:30 pm CST. You may also reply to this email by providing me with the best contact number and time frame for me to give you a call.

These positions do move fast, so time is of the essence. I look forward to hearing from you soon!

Job Title: QC Lab Technician 1

Payrate: $25/Hour on w2

Location: 206 Macks Island Drive, Belvidere NJ 07823

Duration: 12+ months

Shift: 8AM - 4:30 PM Tues - Sat

Description:

Top 3 Skills/Requirements: Analytical skills, communication/people skills, fits well in team environment, attention to detail

Interview Process: preferred 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 -

1. Performs/Applies knowledge and skills to diverse reactions.

2. Release testing of products per current compendia, regulatory and corporate quality systems, and principles.

Position content-

a) Key areas of accountability/responsibility

1. Performs analysis in the laboratory with minimal supervision.

2. Prepares standards, mobile phases, and reagents.

3. Calibrates and monitors laboratory equipment (HPLC, GC, ICP, etc.)

4. Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods.

5. Performs calculations, collects and prepares data for evaluation.

6. Keeps supervisor informed of work status

7. Investigation of OOS results under guidance of senior staff

8. Maintains good documentation practices. SHE Duties & Responsibilities: 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; that area and equipment operate at the highest safety levels; 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.

9. Ensures incidents are investigated, reported, and risks are assessed in a timely basis.

10. Acts in such a way that safety awareness & accident prevention are considered in performing all tasks

11. Shows leadership by working to SHEQ standards and encouraging colleagues to work to the same standards.

12. All employees to be aware of and follow all DSM Life Saving Rules.

13. Shows leadership by working to support Customer Commitments and encouraging colleagues to work to the same standards.

14. Supports plant and corporate initiatives as outlined in the manufacturing plan.

a) Projects/special assignments

1. Responsibility for correctness of the determined results.

2. Work according to SOP's and Specification sheets.

Complexity of the position-

1. Demonstrate the ability to learn and perform lab specific analytical methods

2. Complete analysis on raw materials and finished products within an agreed upon turnaround time.

3. Ensures SOP's and specifications are up to date and in compliance with current Compendia and updates them if required.

4. Performs and documents all work associated in adherence with cGMP guidelines.

Knowledge and educational level -

1. Bachelor's degree in a relevant Scientific discipline preferred, associate's degree required.

2. Broad / General knowledge of quality control techniques and methods.

3. Broad understanding of safety, laboratory hygiene and GMP rules

4. 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 experiences -

1. 0-3 years of lab experience

2. Experience in Microsoft Office (outlook, word, and excel)

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