Lab Technician - Oniste (Urgent Need)

MillenniumSoft Inc; Covington (GA); On-site; USD 30,000 - 42,000; Full time

Job summary

Medical Devices Company is seeking a Lab Technician in Covington, GA on a 6-month contract with a 1st shift schedule, 40 hours/week. Pay rate is $26/hour on W2 contract. Responsibilities include product testing in the complaint laboratory, supporting Quality and Project teams, and ensuring GMP/GLP compliance.

Candidates should have a science-related degree and 1–3 years in a regulated environment. The role requires attention to detail, ability to work in a biohazard environment, and familiarity

Qualifications

• Technical or Associate degree in a science field is a plus.
• Experience in a regulated lab environment is desirable.
• ASQ certification (CQE, CQA, CQM) is a plus.
• Proficiency with MS Excel (pivot tables, v-lookup, etc.)
• 1–3 years of experience in a regulated industry.

Responsibilities

• Represents the Corporation, Division and Quality Department in a professional manner.
• Provides support to Project Teams and Quality Department.
• Responsible for all product testing in the Complaint Laboratory.
• Provides Quality Engineering technical support to resolve quality issues.
• Performs complaint investigations for all UCC and OEM products.
• Creates investigation files in Trackwise.
• Sets up, operates, and maintains laboratory equipment and testing instruments.
• Performs tests and experiments in GMP/GLP.
• Maintains knowledge of ISO and FDA requirements.
• Ensures compliance to Department and Division procedures.

Skills

MS Excel

Laboratory skills

OSHA knowledge

Quality systems awareness

Education

Science-related technical or associate degree

ASQ certification (CQE/CQA/CQM)

Tools

Trackwise

Job description

Client : Medical Devices Company

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

Pay rate: $26/hour

Position: Lab Technician

Location: Covington, GA

Duration: 6 Months

1st Shift

Total Hours/week: 40.00

1st Shift

Client: Medical Devices Company

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

Pay rate: $26/hour

Shift: 9:00am -6pm Monday through Friday

Job Description

• Represents the Corporation, Division and Quality Department in a professional manner.
• Provides support to Project Teams and Quality Department.
• Responsible for all product testing in the Complaint Laboratory.
• Provides Quality Engineering technical support to assist in resolving quality issues, including but not limited to complaint review.
• Performs complaint investigations for all UCC products and as applicable, for OEM manufactured products.
• Creates investigation files in the complaint system (Trackwise).
• Sets up, safely operates, and maintains laboratory equipment and testing instruments.
• Performs tests and experiments in accordance with the requirements of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Develops and maintains a working knowledge of UCC policies and procedures and ISO and FDA requirements.
• Maintains accurate data, analyzes and assists in drawing conclusions.
• Performs tasks accurately and with great attention to detail.
• Must be able to work in a biohazard environment and comply with safety policies and procedures outlined by policies.
• Ensures compliance to Department and Division procedures.
• Interfaces with manufacturing facilities, suppliers, and Product Legal Manufacturer (PLM) groups.
• May present data findings to peers, engineering and management staff.

Education And Experience

• Technical or Associate degree in a science field is a plus
• Prior laboratory experience desirable
• American Society of Quality (ASQ) certification (CQE, CQA, CQM, etc.) is a plus
• Proficiency with using MS Excel (pivot tables, v-lookup, etc.)
• Minimum 1 to 3 years of experience with regulated industry, including co-op/internship experience.

Qualifications

Knowledge and Skills:

• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
• The requirements included in this job description are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Basic knowledge of medical device regulation, industry or international standard.
• Good laboratory skills, along with a working knowledge of laboratory bench methods and associated equipment.
• Understanding of laboratory instrumentation.
• Good understanding of OSHA requirements, Quality Systems Regulations (QSR), Good Laboratory Practices (GLP), ISO, AAMI, and FDA Guidelines, as well as any other regulations/requirements as they pertain to the laboratory.
• Excellent communication skills (verbal, written, and presentation).
• Ability to effectively manage time and manage priorities to meet deadlines.
• Ability to handle multiple task assignments.
• Ability to interpret Corporate, Division and Department Procedures.
• Ability to work with minimal supervision.

Language Skills

• Ability to read, analyze, and interpret general technical procedures or government regulations. Ability to write simple reports and business correspondence.
• Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.

REASONING ABILITY

• This position requires good judgment. All product and process development are to be carried out according to the applicable laws and regulations. When in doubt, the incumbent should source out the appropriate information via internal and external resources.
• Highly variable operations performed daily from complex regulatory and engineering decisions to routine administrative functions. Interpretation of regulations (GMP, ISO 13485, EN46001) into standards and procedures as required. The ability to explain these interpretations to Plant, Division, Corporate and representatives of Regulatory bodies is necessary.
• A great deal of work must be initiated through a detailed knowledge and understanding of the job function, the establishment of plans to attain the end goal.
• Decisions made by this person could have significant regulatory and financial implications. Furthermore, this person’s decisions could have a significant impact on health care practitioners and the welfare of their patients.
• A great deal of work must be initiated through a detailed knowledge and understanding of the job function, the establishment of plans to attain the end goal.
• Decisions made by this person could have significant regulatory and financial implications. Furthermore, this person’s decisions could have a significant impact on health care practitioners and the welfare of their patients.

Physical Demands: (if applicable)

• While performing the duties of this job, the employee is regularly required to sit, walk, talk or hear.
• The employee will sometimes be required to move around in lab environment.
• Specific vision abilities required by this job include close vision and color vision.
• May occasionally lift objects up to 25 lbs.
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Work Environment: (if applicable)

• Minimal exposure to manufacturing environment (i.e. noise, minimal heat and some chemical fume exposure), laboratory, and hospital settings.
• This position works in a normal lab/office environment. The noise level in the work environment is quiet to moderate.
• Work environment requires operating and maintaining laboratory test equipment and measurement instruments.