Technician IV, PM
Company: Disability Solutions
Location: Bloomington
Posted on: October 24, 2024
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Job Description:
Technician IV, PMPosition Summary--Catalent is a global,
high-growth, public company, and a leading partner for the
pharmaceutical industry in the development and manufacturing of new
treatments for patients worldwide. Your talents, ideas, and passion
are essential to our mission: to help people live better, healthier
lives.--Catalent Biologics in Bloomington, Indiana is a
state-of-the art, GMP manufacturing facility, providing one million
sq/ft of drug substance manufacturing, drug product manufacturing,
and related pharmaceutical services. This award-winning facility
helps customers accelerate biologic drug development programs and
bring better treatments to help patients live better, healthier
lives.-----The Technician II, PM requires the coordination and
writing of cGMP manufacturing batch records or batch summary
reports for platform processes. The position responsibilities will
include addressing revisions to the documents, supported by subject
matter experts. --The Manufacturing Sciences and Technology
(MS&T) department's primary function is to serve as an agile
technical services team to support process & technology transfer
(e.g., mAbs, fusion proteins, mRNA, new modalities, etc.),
equipment, consumables, technical writing, and drug substance
lifecycle management.--This position is 1st shift Monday-Friday
8AM-5PM. Position is 100% on site at Catalent's Bloomington,
Indiana facility.Catalent is committed to a Patient First culture
through excellence in quality and compliance, and to the safety of
every patient, consumer and Catalent employee.---- ------ ------
------ ------ ------ ------ ------ ------ ------ ------ ------
--The Role:------- --Responds to internal comments and works with
SMEs to ensure comments are incorporated.------- --Executes
procedures of moderate complexity with high quality with a minimum
degree of guidance.------- --Authors non-process batch production
records (solution, column, bulk fill) to support cGMP manufacturing
with minimal technical understanding.------- --Generates batch
production records in accordance with applicable regulator guidance
and site SOPs.------- --Authors platform documents from execution
batch production records with minimal technical
understanding.------- --Copy-edits documents in accordance with
applicable regulator guidance and site SOPs.------- --Other duties
as assigned.The Candidate:--------- --Associate's degree in STEM
field required; high school diploma required------- --8+ years of
experience in regulated environment/pharmaceutical industry-------
--GMP experience preferred; ability to understand and write
assigned SOPs and moderately complex batch production records with
minimal guidance.------- --Possesses a scientific or writing
background, strong organizational skills, and a high attention to
detail.------- --Applied knowledge of Word, Excel, PowerPoint, and
other and applies technical knowledge to assist and train the site
with Microsoft troubleshooting.------- --Has introductory knowledge
of the principles, theories, and concepts of a discipline.-------
--Requires adaptability, analyzing, assessing, calculating,
decision making, dependability, good judgment, reading, memorizing,
social skills, speaking, stress control, writing.------- --Executes
work plan/schedule developed with input from senior team member;
excellent written communications skills with internal customers;
ability to address work issues at both an individual level and team
level.------- --Ability to communicate effectively and
follow/retain detailed written and verbal instruction in an
accurate, timely, safe, and professional manner with supervisor,
group members, and other departments as necessary, in a
professional and accurate manner.------- --Work environment:
Frequent sitting, standing, walking, reading of written documents
and use of computer monitor screen, reaching with hands and arms,
talking, writing, listening; occasional stooping, kneeling,
crouching, bending, carrying, grasping. Frequent lifting and/or
moving up to 10 pounds and occasional lifting and/or moving up to
50 pounds. --Working in a lab environment will require working with
skin irritants, lung irritants, electrical equipment, sharp
instruments, toxic materials, and hazardous waste. Safety
procedures will be followed to minimize exposure, including clean
room gowning.Why you should join Catalent:------- --Defined career
path and annual performance review and feedback process---------
--Potential for career growth on an expanding team within an
organization dedicated to preserving and bettering lives---------
--Dynamic, fast-paced work environment------- --Generous 401K match
and Paid Time Off accrual--------- --Medical, dental and vision
benefits effective day one of employment--------- --Tuition
Reimbursement--------- --Wellhub program to promote overall
physical wellness--------- --Perkspot - offers exclusive or private
discounts from approximately 900+ merchants in a wide array of
categories--Catalent offers rewarding opportunities to further your
career!-- Join the global drug development and delivery leader and
help us bring over 7,000 life-saving and life-enhancing products to
patients around the world. Catalent is an exciting and growing
international company where employees work directly with pharma,
biopharma and consumer health companies of all sizes to advance new
medicines from early development to clinical trials and to the
market. Catalent produces more than 70 billion doses per year, and
each one will be used by someone who is counting on us. Join us in
making a difference.--personal initiative. dynamic pace. meaningful
work.Visit to explore career opportunities.Catalent is an Equal
Opportunity Employer, including disability and veterans.If you
require reasonable accommodation for any part of the application or
hiring process due to a disability, you may submit your request by
sending an email, and confirming your request for an accommodation
and include the job number, title and location to . This option is
reserved for individuals who require accommodation due to a
disability. Information received will be processed by a U.S.
Catalent employee and then routed to a local recruiter who will
provide assistance to ensure appropriate consideration in the
application or hiring process.--------Notice to Agency and Search
Firm Representatives: Catalent Pharma Solutions (Catalent) is not
accepting unsolicited resumes from agencies and/or search firms for
this job posting. Resumes submitted to any Catalent employee by a
third party agency and/or search firm without a valid written &
signed search agreement, will become the sole property of Catalent.
No fee will be paid if a candidate is hired for this position as a
result of an unsolicited agency or search firm referral. Thank
you.Important Security Notice to U.S. Job Seekers:Catalent NEVER
asks candidates to provide any type of payment, bank details,
photocopies of identification, social security number or other
highly sensitive personal information during the offer process, and
we NEVER do so via email or social media. If you receive any such
request, DO NOT respond- it is a fraudulent request. Please forward
such requests to spam@catalent.com for us to investigate with local
authorities.California Job Seekers can find our California Job
Applicant Notice .
Keywords: Disability Solutions, Greenwood , Technician IV, PM, Professions , Bloomington, Indiana
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