Quality Control Chemist

Integrated Resources Inc.; Rocky Mount (NC); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading company specializing in workforce solutions seeks a Sr. Quality Specialist/Quality Control Chemist for an 18-month contract. This role involves conducting investigations, performing risk assessments, and ensuring compliance with rigorous FDA standards. Ideal candidates will have a Bachelor's degree and 2-5 years of experience in a pharmaceutical environment, demonstrating strong communication and analytical skills.

Qualifications

• 3-5 years' experience in the FDA regulated industry.
• Knowledge of FDA regulations and quality tools.
• Experience in sterile manufacturing.

Responsibilities

• Conduct and write complex formal investigation reports.
• Perform impact risk assessment and assist in root cause determination.
• Evaluate confidential information and develop recommendations.

Skills

Technical Writing

Problem Solving

Communication

Interpersonal Skills

Education

Bachelor’s Degree

Tools

TrackWise

Job description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Job Title: Sr. Quality Specialist/ Quality Control Chemist

Duration: 18 Months

Job Description:

· The Sr. Quality Specialist shall independently conduct and write complex formal investigation reports with input from area SMEs.

· The candidate will function as an independent reviewer of drafted investigations providing constructive feedback and in some instances act as a coach to the investigator.

· This position will also perform impact risk assessment as well as assist in root cause determination and plans appropriate corrective action and preventative action.

· The incumbent will assist in the tracking and trending of corrective and preventative action to assure timely closure.

· This person will also perform reviews and evaluate sensitive, confidential information and develops recommendations for use by the plant quality assurance department.

POSITION RESPONSIBILITIES :

· In order of importance, list the primary responsibilities critical to the performance of the position.

· 2-5 years’ experience in pharmaceutical quality environment required .

· Experience in sterile manufacturing and an understanding of the sterilization process and its impact to products.

· Working knowledge of environmental monitoring and aseptic manufacturing.
Understanding of process validation requirements.

· American Society for Quality (ASQ) certification is an asset.

· Pharmaceutical operations experience and/or knowledge. Experience in a solutions facility preferred.

· Working knowledge of FDA regulations.

· Knowledge of various quality tools such as root cause analysis, DMAIC process, fishbone analysis, etc.

· Prior investigation writing experience (with determination of product impact).

· Strong oral and written communication presentation, interpersonal skills and adept at communication with employees at all levels within the organization.

· Excellent facilitation skills and ability to facilitate strategy meetings.

· Superior technical writing and problem solving skills.

· Organize data, extract key information and write technical summary reports.

· Expertise with word-processing, spreadsheet, and presentation software. TrackWise experience a plus.

ORGANIZATIONAL RELATIONSHIPS:

· Ability to interface with multiple levels of people in the organization, including plant personnel and senior management.

Qualifications

EDUCATION AND EXPERIENCE:

· Bachelor’s degree with 3-5 years experience in the FDA regulated industry.

Additional Information

All your information will be kep t confidential according to EEO guidelines.