RFD_Validation Analyst 1

Posted 15 Days Ago
Be an Early Applicant
Rockford, IL
Entry level
Pharmaceutical
The Role
Responsible for validation project ownership, ensuring compliance, generating protocols and reports, managing quality validation activities, and investigating deviations under supervision.
Summary Generated by Built In

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI. 


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

   

Validation Analyst I (Facility/HVAC Validation Analyst)

Responsible for overall validation project ownership of limited risk project(s) under heavy supervision. Responsible for generation and execution of validation protocols, assistance in audits, and determination of validation needs. This job has no supervisory responsibilities.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Performs validation activities to ensure compliance with government and customer requirements.

Prepares validation protocols, validation statements, reports, summaries, and master validation plans for new customer/product/system project launches and maintains existing validated processes/programs at multiple sites as well as organizing and coordinating internal and customer approvals, as needed. Ensures validation documentation completion, accuracy, and closure, including organizing and coordinating multiple approvals as required.

Prepares change control and validation history report for audits.

Attend conference calls and meetings.

Communicates effectively project goals and progress to Validation Supervisor / Manager.

Investigate validation deviations, document in formal reports, and assure resolution of corrective action to complete project.

Primary contact for quality validation activities and managing expectations. Reviews and interprets standards, procedures and specifications for dissemination relative to validation protocols.

Knowledge of and adherence to all PCI, cGMP, GCP, GAMP, 21CFR, 21CFR Part 11 and Annex 11 policies, procedures, rules, and requirements.

Required to complete and pass a “Documentation Boot Camp” course within 6 months.

This position may require overtime and/or weekend work.

Attendance to work is an essential function of this position.

Performs other duties as assigned. “Limited Risk Projects” are generally defined as projects/customer accounts that have the following.

Business needs of customer/project require standard time commitments.

Low level of uncertainty in managing customer expectations.

Standard validation approach as documented in the Validation Plan. Established criteria that are subject to minimal interpretation.

QUALIFICATIONS:

Required:

High School Diploma or GED and/or 1-3 years related experience and/or training.

Basic Mathematical Skills

Basic Computer Skills: Ability to perform basic computer tasks and operate common computer programs.                                       

Minimum Professional Proficiency: Ability to speak in a way that allows one to participate effectively in various conversations. Ability to read multiple types of standard items addressed to general readers.

Intermediate Reasoning: Ability to apply common sense understanding to carry out instructions that may be furnished in written, oral, or diagram form. Ability to deal with problems that involve several concrete variables in standardized situations.

For candidates in Illinois: This position's base hourly hiring range is $19.95-$22.60 plus an annual performance bonus eligibility. Final offer amounts are determined by multiple factors, including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), a flexible spending account, and 401(k.

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Top Skills

21Cfr
21Cfr Part 11
Cgmp
Documentation Boot Camp
Gamp
GCP
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The Company
HQ: Philadelphia, PA
2,259 Employees
On-site Workplace

What We Do

PCI is a leading provider of integrated pharmaceutical development services to the global healthcare market. With facilities in North America and Europe, PCI supports pharmaceutical and biotech companies with products destined for more than 100 countries around the world. PCI provides services for each stage of the product lifecycle – from early Phase I through commercial launch and long-term supply – and partners with customers to provide key insight and expertise in enabling successful commercialization and bringing lifesaving medications to patients. For more information, go to www.pci.com.

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