Quality Control Specialist 1 (Required Lab Exp and General chemistry background Candidates)

MillenniumSoft Inc; El Paso (TX); On-site; USD 28,000 - 34,000; Full time

Job summary

Medical Devices Company in El Paso, TX is seeking a Quality Control Specialist 1 with a background in general chemistry for a 12-month contract. The role is 40 hours per week, first shift, with overtime as needed.

Requirements include a Bachelor's in Chemistry or Microbiology, hands-on lab training, and familiarity with GLP/GCP/cGMP practices. Experience with USP/ISO/ASTM tests and basic calibration oversight is preferred.

Qualifications

• 3 must haves on the resumes: Laboratory experience, general chemistry background, organization and time management.
• Bachelor's Degree in Chemistry or Microbiology or other related Life Science.
• 2 years in analytical chemistry (preferred).
• Experience in operating GC and HPLC (preferred).
• Familiar with GLP/GCP/cGMP practices.

Responsibilities

• Maintain Quality Reports.
• Perform chemical analysis on drug products to include finish goods and/or stability product.
• Maintain and implement efforts in housekeeping, and safety programs.
• Must have awareness and respect of all company policies and safety rules.
• Maintenance of the Calibration program for laboratory equipment.

Skills

Laboratory experience

General chemistry

Organization

Time management

Education

Bachelor's Degree in Chemistry or Microbiology or Life Science

Tools

GC

HPLC

Job description

Position : Quality Control Specialist 1 (Required Lab Exp and General chemistry background Candidates)

Location : El Paso, TX

Duration : 12 Months

Total Hours/week : 40.00

pay rate-$20-25/hr

1st Shift

Client : Medical Devices Company

Job Category : Quality

Level of Experience : Entry Level

Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)

Shift hours - Mon-Fri / 8am to 5 pm and overtime as needed

3 must haves on the resumes: Laboratory experience, general chemistry background, organization, and time management.

Education - Bachelor's Degree in Chemistry or Microbiology or other related Life Science

Responsibilities

• Maintain Quality Reports.
• Perform chemical analysis on drug products to include finish goods and/or stability product.
• Maintain and implement efforts in housekeeping, and safety programs.
• Must have awareness and respect of all company policies and safety rules.
• Maintenance of the Calibration program for laboratory equipment.

Requirements

• Has an academic background and hands on laboratory training in the field of Chemistry.
• Understands and consistently follows multi-step documented procedures.
• Has hands on experience with USP/ISO/ASTM based chemical testing and performs all testing with strict adherence to the written laboratory work instructions.
• Understands the validation principles for chemical methods, develops and validates new chemical test methods, and prepares study reports as required.
• Maintains accurate and well-organized laboratory records, notebooks and/or worksheets.
• Use theoretical knowledge to interpret data and to trouble-shoot experiments.
• Maintain assigned aspects of the chemistry laboratory work to provide material and technical support.
• With moderate or no supervision, apply comprehensive understanding of defined productivity goals and objectives.
• Maintain appropriate training/certification including GLP and GMP.
• Knowledge of FDA regulations for drugs and device desirable.
• Perform other assigned tasks on as needed basis.
• Must have awareness and respect of all company policies and safety rules.

Qualifications

• Bachelor's Degree in Chemistry or Microbiology or other related Life Science.
• 2 years in analytical chemistry (preferred).
• Experience in operating GC and HPLC (preferred).
• Familiar with GLP/GCP/cGMP practices.
• Excellent communication and interpersonal skills.
• Organized and self-motivated.