Now Hiring! Warehouse Technician and Packers in Malvern, PA 19355

Do you want to do something meaningful? Do you want to help save lives? Manpower is currently seeking Quality Control Biochemists for a well known company that creates flu vaccines!

What's in it for you:

Full time hours
1st/2nd/3rd shift
$17 to $20 per hour based experience
Fast paced - never boring

What the job is:

-Support all Warehousing/Distribution activities associated with shipping product domestically and worldwide, receiving of incoming goods, dispensing of materials to the Packaging Department (including but not limited to Forklift and other Power Equipment Operations) Off
-Shipping Order Entry - including but not limited to entering, verifying or troubleshooting all shipment information, maintaining site addresses, attaching required documents, maintaining appropriate shipping statuses and entering all into the appropriate data bases.
-Pre-shipping/Post Shipping activities - including but not limited to managing all communication intothe warehouse where a shipment is required
-Controlled GMP Filing Area and pulling and reviewing shipping paperwork to assist in shipment related investigations

What you bring to the job:

-1+ years of relevant QA technical experience..
-Create clear, concise detail oriented test plans/cases.
-Ability to understand and create test plans from specifications or verbal communications.
-Industry experience in a cGMP/Quality environment preferred.

Apply To Get In Touch or Learn More:
Choose the option that is most convenient to you to get the conversation started.

Step 1:
· Register as a job seeker on www.manpower.com

Step 2:
· Click Apply to this advertisement
· Email me at [email protected]
· Call a Recruiter: 414-312-5203 ext. 1482
· Text "Malvern" to 414-982-1957 w/ Name & email

Our Client in Merrimack NH is looking for a Quality Control Inspector to join their team! This is a temp to perm position for the right Candidate!

Job Description:
To provide support in carrying out all quality control functions to ensure that quality requirements are met, and perform quality control assignments as required.

Job Functions: (Primary "essential" duties and responsibilities)
* Performs in-process inspection/testing using approved test procedures, quality procedures and visual aids, and documents the results.
* Assists in data entry and performs various electronic transactions.
* Reviews Device History Records (DHRs) for completion and release of non-sterile product.
* Performs destructive testing.
* May perform other various QC testing as needed.
* Contributes to team effort by accomplishing related duties as requested.
* Inspection of some finished goods components per specifications using various measuring devices and documents.

Job Functions (continued): (Primary "essential" duties and responsibilities)
* Provide input to documentation gaps, process improvements.
* Reacts to changing priorities and manufacturing inspection needs with little supervision.
* Assists in special projects as needed.

Required Knowledge, Skills and Abilities: Soft skills and technical requirements to be listed here.
* Demonstrated ability to learn and understand QC core structure (inspection, testing, using various measuring devices, documentation of results, ability to follow DMR).
* Must have a high commitment to safety.
* The ability to perform repetitive tasks with a high level of accuracy.
* Able to work in a controlled clean environment.
* Self-motivated and able to take direction to perform all necessary duties.
* Ability to work cross-functionally with different departments.
* Capable of working in a fast paced, dynamic environment.
* Demonstrates ability to manage time efficiently.
* Strong analytical skills.

Minimum Requirements: minimum requirements for the position.
* High School Diploma or equivalent.
* Minimum of one year of experience working in a QC/GMP/GLP/Manufacturing environment.
* Good computer skills with MS Office applications (Word/Excel).
* Strong communication skills (English)

Quality Requirements (Required language- Please do not edit):
* Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
* Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function).
* Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function).
* Attend all required Quality & Compliance training at the specified interval.
* Adopt the "Beyond Compliance Quality Culture" in the work environment; always meet and exceed requirements.

Environmental/Safety/Physical Work Conditions:
* Duties may be performed in a manufacturing/clean room environment.
* Personal protective equipment may be required as dictated by work environment.
* Must have the ability to work while standing/sitting for long periods of time.

Our Client in Merrimack NH is looking for a 2nd shift Quality Control Inspector I to join their team! This is a temp to perm position for the right Candidate!

Job Description:
To provide support in carrying out all quality control functions to ensure that quality requirements are met, and perform quality control assignments as required.

Job Functions: (Primary "essential" duties and responsibilities)
* Performs in-process inspection/testing using approved test procedures, quality procedures and visual aids, and documents the results.
* Assists in data entry and performs various electronic transactions.
* Reviews Device History Records (DHRs) for completion and release of non-sterile product.
* Performs destructive testing.
* May perform other various QC testing as needed.
* Contributes to team effort by accomplishing related duties as requested.
* Inspection of some finished goods components per specifications using various measuring devices and documents.

Job Functions (continued): (Primary "essential" duties and responsibilities)
* Provide input to documentation gaps, process improvements.
* Reacts to changing priorities and manufacturing inspection needs with little supervision.
* Assists in special projects as needed.

Required Knowledge, Skills and Abilities: Soft skills and technical requirements to be listed here.
* Demonstrated ability to learn and understand QC core structure (inspection, testing, using various measuring devices, documentation of results, ability to follow DMR).
* Must have a high commitment to safety.
* The ability to perform repetitive tasks with a high level of accuracy.
* Able to work in a controlled clean environment.
* Self-motivated and able to take direction to perform all necessary duties.
* Ability to work cross-functionally with different departments.
* Capable of working in a fast paced, dynamic environment.
* Demonstrates ability to manage time efficiently.
* Strong analytical skills.

Minimum Requirements: minimum requirements for the position.
* High School Diploma or equivalent.
* Minimum of one year of experience working in a QC/GMP/GLP/Manufacturing environment.
* Good computer skills with MS Office applications (Word/Excel).
* Strong communication skills (English)

Quality Requirements (Required language- Please do not edit):
* Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
* Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function).
* Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function).
* Attend all required Quality & Compliance training at the specified interval.
* Adopt the "Beyond Compliance Quality Culture" in the work environment; always meet and exceed requirements.

Environmental/Safety/Physical Work Conditions:
* Duties may be performed in a manufacturing/clean room environment.
* Personal protective equipment may be required as dictated by work environment.
* Must have the ability to work while standing/sitting for long periods of time.

Don't let the March winds bite too much-warm up with this great opportunity. Manpower is recruiting for individuals with packaging, labeling, and kit assembly experience. You will be working for a company that combines advance science, expertise and passion to solve serious health issues. They are committed to new thinking and approaches that make a greater impact in over 70 countries by putting people first, breaking the mold, leading by example and making a worldwide impact. Join this company and share in their passion in making lives better around the world for people.

What's in it for you:
Assembly packing and labeling have at least 1-2 years experience. Work schedule is first shift, Monday thru Friday 7 am -3:30 pm. Overtime is optional and offered which includes working until 6:30 pm Monday thru Friday, weekend shifts 6 am - 2:30 pm.

Must have computer skills, packaging, labeling, kit assembly, and documentation experience.

Job description:
* Labeling individual syringes/vials with patient numbers and placing into individual bags/cartons.
* Placing tablets or capsules into bottles and labeling the bottle with individual patient numbers.
* Small kit assembly, such as; placing IV bags and syringes into small cartons and labeling with individual patient numbers.

* Labeling bottles, syringes, cards, and cartons.
* Kit assembly.
* Packing containers into corrugate.
* Filling bottles and blisters using semi-automatic equipment.
* Performing quality checks of documentation, drug product, and commodities.
* Performing some housekeeping duties, and sanitizing work stations.
* Sitting and standing for long periods of time while performing some task.

Stop your job search for an assembly position and apply today at www.manpower.com or call 847-689-2217 to speak to Barbara Beil regarding this position or something else.
We love referrals so please share our job with friends and family.
Also Check out Manpower's career platform with tools and resources to prepare you for today and tomorrow's jobs at www.manpower.com/mypath. While employed with Manpower we pay for your College tuition to further your education.

Do you enjoy the world of chemistry and pharmaceuticals? Are you detailed oriented and looking for a solid career producing high-quality vaccinations?
Manpower is HIRING for a Quality Control Technician in Swiftwater, PA.

What's in it for you?
* Various shifts and departments available (1st, 2nd & 3rd)
* $18.50 - $20.00 per hour plus overtime
* Weekly pay + Direct Deposit
* College assistance program available

What is the job?
* Cross functional tasks including; performing Visual Inspections, Sample Receipt, and Service Area related work.
* Adhering to cGMP requirements.
* Performs tasks as per the testing schedule to meet demands.
* Accurately completes paperwork and documentation.
* Ensures product integrity by testing products, pulling samples, placing work orders, and visual inspection of samples.
* Cleaning and preparing all equipment and safety materials used in other departments.

What do you bring to the job?
* BA/BS in life sciences or High School Diploma
* 2+ years of experience in a cGMP controlled/pharmaceutical industry.
* Will be on feet for entire 8-10-12 hour shift
* Meet background check and drug screening requirements.
* Willing to receive vaccinations. 20/20 vision with corrective eyewear

Apply today www.manpower.com. We love referrals so please share with friends and family. For more information call 631-501-1314

Support the Sample Management, Service Area, and Visual Inspection processes. The selected individual will be responsible for performing the following activities within Quality Control:

* Sample Management via the use of an electronic Laboratory Information Management System (LIMS).
* Service Area work, including autoclave operation, glassware washer use, biohazard waste disposal, and water system sampling.
* Visual Inspections, including performing physical exams on final container product, and reporting results via LIMS.
* Other tasks as assigned.
* Assists with maintaining safety and compliance of the laboratory work area.
* Performs cGMP cleaning of the laboratories, equipment, and ancillary areas as required.

Qualifications
* Ability to work in a dynamic team environment.
* Associates or Bachelors Degree in Biology / Life Sciences required.
* Strong attention to detail
* Experience in a cGMP environment.
* Ability to work in a team environment as well as on an individual basis, and self-motivated individual required.

Preferred Qualifications: Science degree and previous cGMP. Previous Visual Inspection experience a plus.

Requires 20/20 vision- may be achieved with corrective lenses.

Manpower is currently hiring for Order Selectors for one of our clients located in Denver, CO!

This is a Temp to Hire position

Sunday Thursday - 4 pm - until complete

Pay Rate: $17.50/Hour

Job Description:

* Receive and check incoming pick tickets
* Locate products using technology (wristbands scanner and RF scanner)
* Retrieve orders according to quantity, size etc. ensuring accuracy
* Build pallets with orders and position them to loading docks
* Keep records of completed orders
* Adhere to health and safety policies and quality standards

Requirements:
* High School or Equivalent