Quality Control Associate - (Pharma/GMP)

Clinigen; Malvern (Chester County); On-site; USD 50,000 - 70,000; Full time

Job summary

Clinigen Group is seeking a quality-focused professional to ensure compliance with established quality systems by inspecting incoming clinical supplies, labels, and in-process materials. This on-site role requires collaboration across departments and adherence to SOPs and GDP standards.

Strong attention to detail and confidentiality are essential. The successful candidate will perform routine cGMP inspections, prepare supporting documentation, and drive continuous improvement in quality

Qualifications

• High School Diploma or GED required.
• Associates Degree or 2 years equivalent work experience preferred.
• Experience with SOPs, cGMP, or GDP preferred.

Responsibilities

• Perform routine cGMP inspections and disposition of clinical trial labels and materials.
• Prepare documents for cGMP activities.
• Complete in-process inspections to ensure product quality and compliance.
• Collaborate with other departments to identify, investigate and resolve issues.

Skills

Attention to detail

Problem solving

Communication skills

Time management

Confidentiality

Team collaboration

Independent work

MS Office proficiency

Operations collaboration

Education

High School Diploma or GED

Associates Degree or 2 years equivalent work experience

Job description

About Clinigen

Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world.

Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world.

The purpose of this position is to ensure compliance with established quality systems through the inspection of incoming clinical supplies, Clinical Trial labels and in-process materials.

This position requires on-site presence 5 days/week.

To be successful in this role you should have:

• High School Diploma or GED required
• Associates Degree or 2 years equivalent work experience preferred
• Ability to partner with operations/supervisors to identify and correct problems
• Preferred experience with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), or Good Documentation Practices (GDP)

Your role at Clinigen

• Perform routine cGMP inspections, disposition and maintenance of clinical trial labels, incoming clinical trial materials, in-process clinical trial materials, and finished products
• Prepare documents for use in cGMP activities
• Complete in-process inspections during production to ensure products produced meet quality standards and are compliant with established quality systems
• Work with other departments to identify, investigate and resolve issues using problem-solving skills
• Communicates operational and personal concerns and opportunities for improvement to the department leadership
• Know, understand and comply with the company's standard operating procedures and policies
• To follow, promote and enforce relevant SOPs, Job Aids, and Company policies and procedures

We're excited about you if you have:

• Ability to partner with operations/supervisors to identify and correct problems
• Detail oriented and self-motivator who takes the initiative to work independently and with the team
• High regard for confidentiality in dealing with all clients, proprietary and pharmaceutical related information
• Excellent oral and written communication skills and active listening ability
• Excellent time management skills to prioritize work and meet deadlines
• Ability to develop effective working relationships with associates at all levels to influence others and foster a cooperative work environment across the organization
• Highly computer literate; experience operating with all Microsoft Office software

Benefits

While at Clinigen, you'll enjoy:

The culture.

Thanks to our diverse opportunities for engagement and involvement, every colleague's Clinigen experience can be a bit different, and we're proud of that. We work hard to ensure our company culture is inclusive to people from all backgrounds and social styles.

The transparency with leadership.

All colleagues can share anonymous feedback with leadership on a weekly basis through our employee engagement platform. We use this feedback to inform our actions and decisions. We've been able to take steps to continuously improve how we do things at Clinigen.

The benefits.

We take pride in having a broad range of activities, systems, and programs that provide a competitive benefit offering and build a culture of celebrating success.

EEO.

Clinigen is an Equal Opportunity Employer and is committed to providing equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other characteristic protected by applicable law.