Quality Control (QC) Lab Technician

The content and statements documented in this job description are designed to describe the general nature and
level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person
assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job
duties, tasks, skills, and qualifications. The intent of this job description is to be representative of the knowledge,
skills, and abilities needed to satisfactorily perform the essential functions of the position satisfactorily and in
accordance with the established performance expectations.
Duties and Responsibilities
Quality Control (QC) Lab Technician's job duties and tasks include but are not limited to the following:
? Perform sample management for all incoming raw materials, in-process, finished products and stability
samples including but not limited to receipt, logging distribution and destruction and update the status in ILMS
(Laboratory Management System).
? Coordinate chemical and reference standard inventory in the lab, verifying the expired chemicals and
standards and discarding as per company procedures and update all inventories in ILMS.
? Update the stability summary reports after the completion of analytical testing.
? Oversee temperature and humidity monitoring for stability chambers
? Assist in sample loading in stability chambers and submitting stability samples as per schedule.
? Assist in the shipment of the samples to contract labs as required
? Provide general housekeeping in the QC Lab and any other functional activities as assigned by management.
Education and Experience
? Minimum of High School Diploma or equivalent education (ex. GED) and three (3) years of relevant experience.
? Must have good computer skills and proficient user of Microsoft Office Tools to include Word, Excel, Outlook,
PowerPoint, and other lab-related systems.
? Must have excellent communication skills.
? Must be able to clearly communicate in English (verbally and written).
? Must possess a positive, professional attitude toward work and willingness to cooperate with co-workers and
supervisors.
? Metered Dose Inhalation (MDI) pharmaceutical industry experience is preferred.
Working Conditions and Schedule
This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment
is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment,
hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a
pharmaceutical laboratory or manufacturing facility is required.
The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday
work may be requested or required.
Physical Requirements
? Work standing or walking unassisted for 75% or greater of an 8-hour period.
? Able to wear appropriate personal protective equipment, when required.
? Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.
? Able to lift 35 pounds with or without assistance.
? No remote work available.

Professional and Behavioral Competencies
? Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be
Monday to Friday.
? Must be willing to work some weekends based on business needs as required by management.
? No remote work available
? No employment sponsorship or work visas.

• Must Haves:

• Minimum High School Diploma or advanced training or education in pharmaceutical quality compliance or related field of study from an accredited college/university.is preferred.

• Minimum of three (3) years’ experience in quality assurance in a current Good Manufacturing Practice (cGMP) pharmaceutical work environment.

• Experience in metered dose inhalation (MDI) preferred.

• Proficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP, and other business applications.

The Hiring Manager for this role only wants to consider candidates with the requisite experience and education in quality assurance work preferably in the pharmaceutical industry.

Job Type: Full-time

Salary: $40,000.00 - $54,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Relocation assistance
• Vision insurance

Schedule:

• 10 hour shift

Ability to commute/relocate:

• Alma, MI 48801: Reliably commute or planning to relocate before starting work (Required)

Experience:

• CGMP: 1 year (Required)
• Quality control: 1 year (Required)
• Pharmaceutical: 1 year (Required)

Work Location: One location

Salary : $40,000 - $54,000