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Overnight Operative Iq Jobs (NOW HIRING)

Genesis AEC, Inc.

Validation Engineer I

Orange, CA · On-site

$60 - $70/hr

... operated to meet design and owner requirements. The selected candidate will be responsible for ... Write and perform CQV documentation [Commissioning / IQ/OQ/PQ protocols for various types of ...

Canon Medical Systems

Remote Support Engineer -XR/VL

$86K - $138K/yr

Operating within a 24/7 support environment, this role requires flexibility to work rotational ... Work day, evening, and overnight shifts on a rotating basis * Participate in a rotating weekend and ...

Danaher

Senior Product Engineer

Westborough, MA · On-site

$105K - $125K/yr

At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a ... Experience implementing process validation procedures and techniques, such as IQ, OQ & PQ, process ...

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Infographic showing various Overnight Operative Iq job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 21% Part Time, and 1% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution.

Sanitization Technician / 3rd shift / Pharma Industry

Pioneer Data

Andover, MA • On-site

$19.25 - $25.50/hr

Contractor

Re-posted 25 days ago

Job description

Position Details: 
Our client, a world-leading Pharmaceutical Company in Andover, MA is currently looking for a Sanitization Technician to join their expanding team.
 
Job Title: Sanitization Technician / 3rd shift / Pharma Industry
Duration: 12 months contract, extendable up to 48 months
Location: Andover, MA
 
Note: 
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
 
Job Description:
Summary:
The main function of a Process Development Technician is to support the design, testing, and optimization of manufacturing or laboratory processes.
A typical Process Development Technician works closely with engineers and scientists to implement new procedures, troubleshoot equipment, and ensure process efficiency and compliance.
 
Key Responsibilities
The selected contractor will:
Attend a 9:00 PM shift huddle to receive nightly assignments.
Perform sanitization and cleaning activities within laboratory/manufacturing areas.
Sanitize:
Floors
Countertops
Drains
Walls (monthly cleanings)
Safety showers
Use cleaning equipment such as walk-behind scrubbers and Matador scrubbers (training provided).
Complete required GMP and site-specific training.
 
Training & Onboarding
Extensive onboarding and training will be provided.
Employees are paired with a trainer until they can independently perform all assigned tasks.
Typical training period may last several months.
No prior GMP experience is required.
 
Candidate Profile
Must-Haves
Ability to reliably work overnight (3rd shift).
Basic computer skills.
Ability to stand for extended periods.
Ability to perform light physical work, including lifting/moving 20–30 lb buckets.
 
Experience Requirements
Manager considers the role truly entry-level.
Preferred experience range: 1–2 years or more.
Prior sanitization, pharmaceutical, GMP, or manufacturing experience is a plus but not required.
Strong willingness to learn is more important than specific technical experience.
Equipment & Physical Requirements
Use of 4- to 6-gallon buckets weighing approximately 20–30 pounds.
Frequent standing and movement throughout the shift.
No machinery disassembly or maintenance responsibilities.
 
Key Takeaway
The primary recruitment challenge is finding dependable candidates willing to work a permanent overnight shift. The role is highly trainable, requires minimal prior experience, and focuses on sanitization activities within a GMP-regulated environment.
 
 
Job Responsibilities:
Assist in the development and scale-up of new manufacturing or laboratory processes Operate, calibrate, and maintain process equipment and instrumentation Collect and analyze data to evaluate process performance and identify improvements Document procedures, results, and standard operating protocols (SOPs) Support validation activities including IQ/OQ/PQ testing Collaborate with cross-functional teams to meet project goals and timelines
Ensure compliance with safety, environmental, and quality regulations Train operators and technicians on new or revised processes
 
Skills:
Strong mechanical and technical aptitude Ability to interpret technical drawings, schematics, and process documentation
Proficiency in data analysis and process simulation tools
Excellent problem-solving and troubleshooting skills Effective communication and teamwork abilities Familiarity with GMP, ISO, or other regulatory standards
 
Education/Experience:
Associate degree in Engineering Technology, Industrial Science, or related field preferred 2-4 years of experience in process development, manufacturing, or laboratory support