Quality Control Lead

Polysciences, Inc; Warrington Township (Bucks County); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Medical Plans

Dental Plans

Vision Plans

401(k) with company match

Paid Time Off

Year-end Bonus

Job summary

Polysciences, Inc. is seeking a Quality Control Lead to coordinate in‑process, intermediate, and finished product testing and to mentor QC Analysts. The role supports manufacturing and product release in an ISO13485/FDA GMP environment.

You will schedule tests, review data, investigate OOS results, and ensure an organized lab with 5S standards while driving Six Sigma and Lean initiatives.

Qualifications

• Bachelor's degree in Chemistry or related field required.
• Six Sigma or related certification required.
• Auditor (CQA) or related certification preferred.

Responsibilities

• Lead the quality control team and provide hands-on training.
• Coordinate testing of raw materials, in-process, intermediates and finished goods.
• Review QC data, investigations and ensure data integrity across lab systems.
• Maintain 5S and drive continuous improvement initiatives.

Skills

Leadership

Mentoring

GMP compliance

Education

Bachelor's Degree in Chemistry

Six Sigma Certification

CQA Certification

Tools

GC-MS

LC-MS

NMR

DSC

TGA

Job description

Polysciences technical operations and scientific laboratories offer custom synthesis, contract manufacturing and packaging, and laboratory products. We are proud to offer a broad range of products and tailored solutions for the life sciences, bioprocessing, microparticles, medical devices, specialty chemical and eChem industries. We adhere to ISO13485:2016, FDA cGMP 21 CFR 820 regulations, and SOCMA’s ChemStewards Management System. We believe the best scientific innovations are built through collaborations.The Quality Control Lead is responsible for scheduling in-process samples, intermediate products, final products, and stability samples analytical analysis to support both product manufacturing and commercial product release needs. Serves as liaison between production, planning, business with the QC department for analytical activities needs. QC Lead is also responsible to mentor QC Analysts to ensure department’s compliance to the QC Laboratory Systems such as equipment maintenance, OOS Investigations, Inventory, Activity Logbooks, etc.Essential Functions:Provide leadership and guidance to the quality control team, including on-hands training, and mentoring.Coordinate work assignments for raw materials, in-process, intermediates and finished goods samples testing. Prioritize testing schedule to ensure efficient operation of the quality control department and adherence to KPIs.Foster a culture of accountability, collaboration, and continuous improvement within the teamLeads other QC Analysts on laboratory inventory maintenance to ensure no impact to TAT. Assist on inventory sourcing along with Procurement Department when necessary. Escalates any potential issues to QC Manager in a timely manner.Independently performs equipment maintenance as well as equipment and software troubleshooting.Independently reviews of QC data, using both electronic systems and hard copy documentation as well as QC Orders Completion.Reports OOS results, compiles required information and independently completes laboratory investigation reportIndependently review, revise, and approve procedures and test methodsMaintains a safe, clean, and organized environment (5S) for all QC areas. Ensures adherence to 5S audit schedule.Implement quality and continuous improvement initiatives, such as Six Sigma, Lean Manufacturing, or Total Quality Management principles.Engage cross-functional teams to implement best practices and foster a culture of continuous improvementWhen required, perform routine analytical analysis using the following equipment: volumetric glassware, balances, GC-MS, GC-FID, LC-DAD, LC-MS, NMR, TGA, DSC and others as required.Serves as QC Manager designee for approval, QC related investigations, protocols, reports, procedures and instructions.Qualifications:Bachelor’s Degree in Chemistry or related science field required.Six Sigma or related certification required.Auditor (CQA) or related certification preferred.At least five (5) years of experience working in an ISO 13485 or FDA GMP regulated environment required.Proven leadership abilities or training on coaching, mentoring, and team-building skills.Experience with quality control GMP documentation of testing results and assurance of laboratory data integrity and compliance required.Strong knowledge of analytical equipment, analytical methods, method validation and data analysis required. Knowledge of compendial methods (ie. USP, EP, ISO, ASTM) required.Knowledge on ICH guidelines preferred.What We OfferCultureGreat peoplePeer to Peer RecognitionBroader, hands-on work experienceClean and Modern Equipment & LabsFun company eventsCompetitive Wages & Generous Year-end BonusComprehensive BenefitsMedical Plans with Telemedicine, Rx, & Vision2 Dental PlansHealthcare, Dependent care, & Commuter Flexible Spending Accounts401(k) with company matchFinancial Health & Wellness w/1:1 Coaching & RewardsBasic & Supplemental Life InsuranceAccident, Hospital Indemnity, & Critical IllnessPaid Time OffPaid Parental LeaveShort & Long-term Disability9 Paid HolidaysMust have legal authorization to work in the US and will not require sponsorship.Polysciences is an equal opportunity employer. Drug-free workplace. Tobacco-free work site.Polysciences does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit and business need.Equal access to programs, services, and employment is available to all persons. Those applicants requiring reasonable accommodation to the application process and/or interview process should notify a representative of the Human Resources Department.Find us here Poly 424QualificationsEducation Required: Bachelor's Degree Preferred: Choose an item.Certification(s): Specify preferred or required.Bachelor’s Degree in Chemistry or related science field required.Six Sigma or related certification required.Auditor (CQA) or related certification preferred.Computer Skills Required: Specify preferred or required.Proficiency with Adobe, Microsoft Word and, Excel.Other qualifications:At least five (5) years of experience working in an ISO 13485 or FDA GMP regulated environment required.Proven leadership abilities or training on coaching, mentoring, and team-building skills.Experience with quality control GMP documentation of testing results and assurance of laboratory data integrity and compliance required.Strong knowledge of analytical equipment, analytical methods, method validation and data analysis required.Knowledge of compendial methods (ie. USP, EP, ISO, ASTM) required.Knowledge on ICH guidelines preferred.Immediate Work Environment:X- Chemicals Unprotected Height X- Fumes/Gases Persistent NoiseX- PPE used: Lab Coat, Safety Shoes, and Safety GlassesWork Activity: [must equal number of hours worked per day]Stand: 3 Frequency: Intermittently Walk: 1 Frequency: IntermittentlySit: 4 Frequency: Intermittently Drive: 0 Frequency: Choose an item.Lift/Carry DemandsFrequency: Lift/Carry Equipment Provided:0-10 lbs. 1-3 hours a day Reagents Bottles Carriers11-25 lbs. Not Daily Rolling Cart26-50 lbs. Rarely Gas Tank Hand Cart/Drum Lift Cart51-75 lbs. Choose an item. Click or tap here to enter text.76-100 lbs. Choose an item. Click or tap here to enter text.