Quality Control Production Supervisor
Englewood Lab, Inc. · Totowa, NJ
- Level
- Supervisor
- Team
- Quality
- Base pay
- $65k–$75k
- Degree
- Required
- Industry
- Industrial
- Posted
- 27 days ago
The role in 30 seconds
A supervisor quality role at Englewood Lab, Inc. (industrial) in Totowa, NJ.
- They ask for
- degree required
- Tools it names
- ISO 13485, FDA / GMP, Internal audits, Assembly lines, EHS / safety
- Base pay
- $65k–$75k
- Day to day
- some off-shift / weekend coverage
Read from the posting. The full description is below.
How this role compares
Against 7 other live quality postings in New Jersey.
Skills these teams ask for most
- ✓ FDA / GMP 63%
- ✓ Team leadership 38%
- SPC 25%
- SAP 25%
- ✓ Internal audits 25%
✓ = this posting asks for it too. % = share of similar postings that mention it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at Englewood Lab, Inc.
Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
- 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- How does off-shift and weekend coverage work?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
Full description from Englewood Lab, Inc.As posted on their careers site.ShowHide
requirements
(e.g. FDA, EPA, OSHA, ISO 13485:2003).
- ✓Reviews finished goods with shipping department for formal FGs release and compliance to customer requirements.
Responsibilities
- ◆Work closely with Quality Assurance/Quality Systems Dept on all aspects of Quality and Compliance.
- ◆Maintains a working knowledge of QC inspection
requirements
for components, raw materials, in-process/bulk and finished goods.
- ✓Ensures that review of in-process activities in Manufacturing or Production/Assembly areas is conducted by QC inspectors for conformance to specifications; follow up on out-of-specifications including non conformances.
- ✓Participates in In-process Quality in-house and outside training program.
- ✓Conducts periodic analysis of In-process Inspection program and makes recommendations.
- ✓Assist in interpreting and/or developing of customer specifications and
requirements
for assembly/packaging specifications.
- ✓Assists in establishing production and assembly inspection information sheets and documentation as required
- ✓Maintains and updates ERP System, maintains repository of batch records/documents, and other Mfg & Assembly in-process Specifications.
- ✓Reviews of batch records, work sheets, and Inspection documentation for completeness and correctness.
- ✓Conduct non-conformance resolutions, complaint investigations, and associated corrective and preventative actions.
- ✓Reviews of QC Inspection reports daily for correctness and completeness.
- ✓Facilitates on site customer inspections, coordinating availability of product and communication of disposition to Quality and Inventory Control. Interfaces with customer distribution operations where needed.
- ✓Maintains awareness and compliance with safety regulations in performing job duties.
- ✓Reviews Production and in-process related information on batch records/documents.
- ✓Ensure that finished goods, bulk, raw materials, components are maintained correctly in the warehouse and other holding areas.
- ✓Assist in the review and release of finished products.
- ✓Perform supplier and vendor audits, as well as, Mock recall and internal audits
- ✓Any additional duties of assignments as directed by the Supervisor.
Qualifications
- ✓Minimum of Diploma or Bachelor degree (Life Sciences, Engineering, relatedprofession)
- ✓Five+ years industry or related experience in cosmetic, device, food, or pharma.
- ✓Previous inspecting, auditing or manufacturing experience - a plus.
- ✓Data analysis, specification development skills.
- ✓Computer literate and effective communication skills.
Show full description ↓Show less ↑
Quality Control Supervisor
Location: Totowa, NJ (Onsite)
Employment Type: Full-Time | Exempt
Department: Quality Control
Reports To: Manager / Director of QC
Supervises: Quality Control Associates, QC Leads & Inspectors
Organizational Relationships: Contact with all areas of QA/QC personnel, Customers, Production Supervision, Warehouse, Engineering, and Operational personnel
Basic Functions
- •Scheduling of QC Inspectors to one of the following areas: (i) Bulk Mfg with Review of In-process Batch Records and related documentation and Special Sample handling, OR (ii) Production areas/Assembly lines, Warehouse FG auditing, Special Sample handling, Review of In-process Fill/Assembly Records and related documentation.
- •Conduct non conformance, product complaints, out-of-specification investigation and provide corrective and preventive actions with follow-ups within specified area(s).
- •Trains and supervises document review personnel; batch release personnel, issues certificates of conformance (COC), certificates of manufacture (COM), and certificates of analysis (COA) to customers on finished goods. Maintains accurate record of approved, quarantined, rejected products within specified area(s).
- •Ensure compliance to all SOPs and other regulatory
Work Schedule
- •Onsite position based in Totowa, New Jersey.
- •Monday through Friday, Full-Time.
- •Additional hours may be required to support audits, inspections, regulatory submissions, and business needs.
$65,000 - $75,000 annually
Benefits
- •Medical, Dental & Vision Insurance
- •Company-paid Life, AD&D and Disability Insurance
- •401(k) with Company Match
- •Paid Time Off (PTO)
- •Paid Company Holidays
- •Special Paid Leave for Personal Events
- •Employee Referral Program
- •Additional benefits as outlined in the Employee Handbook