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Quality Control Associate Two Jobs in Rhode Island

Careers | CET

Quality Associate

Bristol, RI

Summary The Quality Associate supports both quality assurance and quality control initiatives regarding Production and Operations to ensure that customer requirements are met, and any discrepancies ...

Veranex

Logistics Associate 2

Providence, RI · On-site

$17.02 - $24.33/hr

Complete all related transactions in the Inventory Control System. * Receive incoming packages, verify packing slips, and manage loading and unloading of deliveries. Distribute packages to ...

Nordsonhcm

Warehouse Associate II

East Providence, RI · On-site

$16 - $19.25/hr

We offer hourly and salary positions in production, maintenance, customer service, quality, engineering, and more. We actively invest in our teams to help you build your skillsets and advance your ...

New

Cadence Inc

Quality Inspector, 2nd Shift

Cranston, RI · On-site

High school diploma or equivalent; associate degree in a related field preferred. * Proven experience in quality control or quality assurance within a manufacturing environment. * Familiarity with ...

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All JobsQuality Control Associate Two JobsQuality Control Associate Two Jobs in Rhode Island

Quality Control Associate Two information

What is the difference between Quality Control Associate Two vs Quality Control Associate One?

AspectQuality Control Associate TwoQuality Control Associate One
Required CredentialsHigh school diploma or equivalent; some roles may require certifications in GMP or ISO standardsHigh school diploma or equivalent; basic understanding of quality standards
Work EnvironmentManufacturing or laboratory settings, often in regulated industriesSimilar environments, typically in labs or production areas
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing companiesCommonly used in similar industries, often as entry-level roles
Common Search & Comparison IntentYes, often compared to associate level roles to understand responsibilities and requirementsNo, usually the starting point for quality roles

Quality Control Associate Two typically requires more experience or certifications than Quality Control Associate One. It involves more responsibilities in quality inspections and compliance, making it suitable for those with some industry experience. Both roles are common in manufacturing and laboratory environments within regulated industries.

What cities in Rhode Island are hiring for Quality Control Associate Two jobs? Cities in Rhode Island with the most Quality Control Associate Two job openings:
Quality Control Associate Two jobs near you
QC Scientist II, Analytical Chemistry (3rd shift)

QC Scientist II, Analytical Chemistry (3rd shift)

Pharmaron

Coventry, RI • On-site

$75K - $95K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted just now

Job description

Position: QC Scientist II, Analytical Chemistry (3rd Shift)
Salary Range: $75,000-$95,000
Location: Coventry, RI
About Pharmaron
Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programs, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit .
Job Overview:
This position will support manufacturing and process chemistry activities through analytical method validation, transfer, sample testing and ensuring QC lab in compliance with all applicable guidelines.
3rd shift, working hours: 11:00 pm- 7:30 am. Must be open to working 2nd shift (3pm -11:30am) as business requires.
Key Responsibilities
  • Sample raw materials and conduct QC testing of raw materials, intermediates, API, IPC and cleaning verification samples following established procedures.
  • Document and report results of all experiments in a timely-manner consistent with department practices and governing procedures, as applicable.
  • Participate in method transfer or validation activities, including executing the protocols and preparing the reports.
  • Review experimental data, notebooks, and instrument qualification protocols / reports.
  • Write, revise, develop, and evaluate SOPs.
  • Maintain good laboratory practices and GMP in compliance with safety and environmental requirements.
  • Ability to work successfully in both a team/matrix environment as well as independently.
  • Report lab event or deviation and participate in the investigation.
  • Ensure high quality in QC and analytical work and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.
  • Provide training to other team members on instrument and testing method.
  • Participate, support and facilitate site audits as directed and required.
  • Perform other related assignments and duties as required and assigned.

What We're Looking For
  • BS or MS degree in chemistry or related field
  • 2+ Years of pharmaceutical industry experience
  • Ability to perform routine QC work independently with minimal guidance
  • Proven skills in analytical method verification and validation of small molecules
  • Effective in managing multiple competing activities and delivering to timelines
  • Ability to work in a cross-function environment
  • Experience in HPLC, GC, FTIR, UV and wet chemistry
  • Working knowledge of cGMP and applicable FDA, EMA and ICH guidance
  • Excellent communication skills, both verbal and written

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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