Manufacturing Technician II - Inspection (Days)

BioSpace

Olde West Chester (OH)

On-site

USD 29,618 - 44,083

Full time

14 days+

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Benefits offered by this job

Annual cash bonus program

401(k) with company match

Healthcare benefits

Flexible time off

Job summary

A leading biomanufacturing company in Ohio is seeking a Manufacturing Technician II to join their Inspection Process Execution Team. This full-time position involves operating equipment, performing inspections, and maintaining documentation in accordance with cGMP standards. Candidates with experience in pharmaceutical manufacturing who can adapt to fast-paced environments are encouraged to apply. This role promises a competitive hourly pay between $21.50 and $32.00, depending on experience and qualifications.

Qualifications

Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language.
Experience in a cGMP regulated environment is necessary.
Good attention to detail is required.

Responsibilities

Operate machinery and perform inspections as required.
Document batch records and maintain logs.
Support process improvement activities.

Skills

Attention to detail

Effective communication

Ability to work in teams

Adaptability

Education

Experience in pharmaceutical or cGMP environments

Tools

SAP

Job description

Manufacturing Technician II - Inspection (Days)

Join to apply for the Manufacturing Technician II - Inspection (Days) role at BioSpace

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit www.resilience.com

Brief Job Description

The Manufacturing Technician II reports to a Manager/Supervisor in the Inspection Process Execution Team (PET) operations. This position will require working in various Controlled/Non-Classified areas. The Technician performs a variety of manufacturing tasks (operates equipment, performs visual, cosmetic, and physical inspection, line clearances, OEE data collection and completes batch record entries) and supports improvement activities (5S, participate in problem‑solving and Kaizen events, manual data collection) in accordance with cGMPs.

Primary Responsibilities

Perform the duties of operating assigned machinery consisting of servicing automated inspection equipment, monitoring equipment status, reintroduction of materials, manually palletizing inspected materials, and assuring a smooth flow of product.
Perform manual visual, cosmetic, and physical inspection of material. Promptly escalate concerns to Lead and Manager/Supervisor as needed. Must obtain and maintain visual inspection qualification.
Be able to start up equipment, make minor adjustments to machinery, remove jams, minor troubleshooting, and minor assembly/disassembly for cleaning purpose.
Ability to use material handling equipment such as motorized and manual pallet jacks, non‑motorized lifts.
Perform cleaning, housekeeping and line clearance activities for assigned areas as required to maintain a cGMP environment.
Perform batch record and GMP documentation entries. Maintain records and/or logs as required in the performance of job responsibilities. This will include mathematical computation where needed.
Knowledge of product security controls and material handling equipment.
Responsible for outgoing quality level.
Be familiar with job‑related safety procedures and hazards including PPEs, ergonomics, LOTO, human safety, material handling, waste handling, chemical handling, and spill controls. Report all discrepancies to process facilitator.
Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety procedures in accordance with OSHA requirements and guidelines. Be familiar with “Material Safety Data Sheets” for area chemicals.
Obtain knowledge to be able to print off SOP’s/Forms via ECMS.

Other Responsibilities

Support lean activities and process improvement work such as performing 5S in the work area, participating in problem‑solving, and manual tracking of performance data for OEE and process improvement analysis.
Review process documents such as operational SOPs, forms and batch records for accuracy. Identify and provide suggestions for process improvement while maintaining quality and cGMP compliance as opportunities arise.
Be flexible and support other work areas as needed
Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee as needed.

Optional Training / Responsibilities

Obtain cold room training/access to be able to transfer materials in and out of the cold rooms.
Take proper training to become certified trainer on assigned equipment and process tasks. Train and conduct evaluations on other team members for training qualifications.
Obtain a novice to intermediate level of knowledge of SAP inventory movements and inventory management such as moving items from one storage location to another and goods issuing items to process orders as required.

Competencies & Job Requirements

Acquire and maintain all required certifications and qualifications for the assigned work area
Capable and motivated to learn new skills and develop new capabilities on an ongoing basis to contribute to the success of the Process Execution Team
Ability to work effectively in a team environment
Candidate should possess the ability to work in and adapt to a changing/demanding environment
Some overtime may be required with minimal advance notice to support business needs

Minimum Qualifications

Experience in a pharmaceutical or cGMP regulated environment
Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language.
Good attention to detail is required. Individual must be capable of keeping accurate records and performing mathematical calculations.

Preferred Qualifications

Prior production experience
Experience working in a LEAN manufacturing environment
Knowledge of cGMPs and FDA policies/procedures
Prior inspection experience in a pharmaceutical manufacturing environment.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non‑job‑related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.

Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $21.50 - $32.00 per hour. Actual base pay is dependent upon a number of factors, including but not limited to the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

Seniority level