Quality Control Analyst

Staffing Resource Group, Inc; Quakertown (Bucks County); On-site; USD 30,000 - 47,000; Full time

Job summary

Staffing Resource Group, Inc. seeks a Quality Control (QC) Analyst for our pharmaceutical client in Quakertown, PA. The role executes routine analytical testing of raw materials, intermediates, and finished products, documenting results and maintaining lab records.

Training shifts run 1:30pm–11:30pm; post-training, a 4:30pm–2:30am schedule is expected, Mon–Thurs. Associates degree or higher preferred; GMP/Quality experience and HPLC expertise are advantageous.

Qualifications

• GMP or Quality experience preferred.
• HPLC experience preferred.
• Microtrac (Particle Size) preferred.
• Basic computer skills required.
• Strong communication skills both verbal and written required.

Responsibilities

• Test raw materials, intermediates and finished products and record results.
• Maintain lab records and data; ensure accuracy of data and documentation.
• Support method transfer and validation experiments and regulatory compliance tasks.
• Assist with investigations and general lab support as needed.

Skills

GMP/Quality experience

Strong communication skills

Basic computer skills

Safety procedures

Quality testing mindset

Education

Associates degree or higher

Tools

HPLC

Microtrac

Job description

Quality Control Analyst Title: Quality Control (QC) Analyst

Location: Quakertown, PA

Industry: Pharmaceutical

Salary: $25/hr. + 10% Shift Differential

Schedule: Training Hours will be 1:30pm-11:30pm, Mon-Thurs. After training period of 60-90 days, QC Analyst will then work from 4:30pm-2:30am, Mon-Thurs.

Employment Type: Direct Hire

Company Overview: Operating from a 100,000 square foot, US-based, state-of-the-art, FDA inspected facility, this company has the experience and capabilities to rapidly develop, scale up, and process APIs and excipients ranging from grams to multi-metric tons, including highly potent compounds.

Job Overview: The Quality Control Analyst is critical to the Company s success in providing a quality service to our customers in a timely fashion. This position carries out the practical work in the laboratory such as routine analytical testing. Performs required testing on raw materials, intermediates and finished products. May support Quality management to provide method technology transfer and project preparation. Follows GLP and cGMP procedures and documenting actions.

Job Description: Testing of raw materials, intermediates and finished products Records test results and maintains raw data and accurate laboratory recordsMaintain lab assets in accordance with written procedures & regulatory requirementsApprove or reject finished product samplesGeneral lab support including housekeeping, equipment maintenance, inventory of supplies, etc.Runs analytical method transfer and validation experiments.Assist on preparation work of projectsAssist on the OOS investigationsProvide technical support and answers during the analysis of production sampleAssist with various duties when needed as instructed by supervisor

Education: Associates degree or higherGMP or Quality experience preferredHPLC experience preferredMicrotrac (Particle Size) preferredBasic computer skillsStrong communication skills both verbal and written required

Essential Job Functions: Must understand and follow job safety procedures at all timesAdherence to cGMPs is required at all times.Majority of role is laboratory based and must abide by good laboratory practices.Wear PPE as required.Must accurately record process details.Ability to multi-task in a fast-paced manufacturing environment.Must be able to lift 30lbs

Why Join Us: Consistent weekday schedule with paid breaks & opportunities for overtimeGain hands-on experience with cutting-edge pharmaceutical technologiesWork in a facility trusted by top pharmaceutical and biotech companies worldwideGreat entry point into the pharmaceutical industryJoin a collaborative team where safety, quality, and continuous improvement come first

EOE/ADA IND123