Notifications

Are you open to new opportunities?

Upload your resume to increase your chances of getting noticed.

Ultragenyx
3.4
Manufacturing Associate II - Upstream - Day Shift (Pitman schedule)
Bedford, MA
$78K - $97K (Employer provided)
Ongoing maintenance of own training file ensuring full training has taken place for all aspects of the production activities in the GTMF area.…
30d+
Sallie Mae
3.9
Senior Associate, Internal Audit
Newark, DE
$86K - $116K (Glassdoor est.)
3+ years of experience in internal audit, external audit, or a related field. Bachelor's degree in accounting, finance, or a related field.…
30d+
internal auditor jobs in Newark, DE Newark, DE jobs Sallie Mae jobs in Newark, DE
Sallie Mae salaries internal auditor salaries in Newark, DE
Employee reviews at Sallie Mae Sallie Mae interview experience Working at Sallie Mae
gpac
3.0
Audit Associate / Audit Senior / Audit Manager
Indianapolis, IN
$65K - $110K (Employer provided)
Easy Apply
Certifications: Started the process of obtaining a CPA license; having sat for and/or passed at least one section of the exam is preferred.…
10d
OmniForce Solutions
5.0
Senior Audit Associate
Houston, TX
$71K - $95K (Glassdoor est.)
Easy Apply
4-5 years of public accounting audit experience, a CPA license or active CPA candidacy, and demonstrated experience with financial statement preparation.…
26d
Kearney & Company
4.2
IT Audit Senior Associate (TS/SCI w/ Poly Required)
Fort Meade, MD
$60K - $100K (Employer provided)
Bachelor's degree in Accounting, IT, or relevant technical field of study. Kearney and Company is seeking an IT Audit Senior Associate to apply technical and/or……
30d+
Kearney & Company
4.2
Senior Audit Associate (TS/SCI w/ Poly Required)
Fort Meade, MD
$60K - $100K (Employer provided)
Bachelor's degree in Accounting or relevant business or technical field. Provide input to methodology while coordinating analysis with other project personnel.…
30d+
Kearney & Company
4.2
Senior Audit Associate (TS/SCI w/ Poly Required)
Fort Meade, MD
$60K - $100K (Employer provided)
Bachelor's degree in Accounting or relevant business or technical field. Provide input to methodology while coordinating analysis with other project personnel.…
30d+
OmniForce Solutions
5.0
Senior Audit Associate
Dallas, TX
$74K - $96K (Glassdoor est.)
Easy Apply
4-5 years of public accounting audit experience, a CPA license or active CPA candidacy, and demonstrated experience with financial statement preparation.…
26d
Leoforce
4.0
Audit Senior
Burbank, CA
$150K - $200K (Employer provided)
Easy Apply
Manage, develop, train, and mentor staff on projects and assess performance for engagement and year-end reviews. Bachelor’s degree in accounting.…
22d
Selby Jennings
3.5
Senior Auditor
Dallas, TX
$105K (Employer provided)
Easy Apply
Bachelor's degree in accounting, finance, or related field; relevant certifications (CPA, CIA) preferred. As a Lead Auditor, you'll work across various key……
2d
FHLBank Chicago
3.2
Senior Auditor
Chicago, IL
$90K - $151K (Employer provided)
Easy Apply
Certified Internal Auditor (CIA), Certified Public Accountant (CPA) or some other relevant certification or working towards certification.…
12d
ASGN Incorporated
3.5
Audit Senior
Greensburg, PA
Easy Apply
Bachelor's degree in Accounting or a related field. CPA eligible or currently pursuing CPA certification is preferred.…
5d
Crowe LLP
3.7
Audit Senior Associate - Life Science
Boston, MA
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
Distinct Recruitment
4.8
Senior Audit Associate
Deerfield, IL
$80K - $95K (Employer provided)
Easy Apply
You'll lead audit engagements from planning through completion, review work prepared by junior staff, mentor less experienced team members, work directly with……
3d
Crowe LLP
3.7
Audit Senior Associate - Insurance
Hartford, CT
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
ASGN Incorporated
3.5
NFP Audit Senior
Lutherville Timonium, MD
$85K - $100K (Employer provided)
Easy Apply
Certification: CPA license is not required, but actively pursuing it is preferred. Supervise and mentor junior staff auditors during field assignments.…
4d
ASGN Incorporated
3.5
Audit Senior
College Station, TX
$70K - $95K (Employer provided)
Easy Apply
CPA license or active pursuit of CPA certification preferred. Assist with risk assessments and understanding clients business operations and internal controls.…
5d
ASGN Incorporated
3.5
Audit Senior
East Brunswick, NJ
$85K - $110K (Employer provided)
Easy Apply
Strong technical audit skills and thorough understanding of audit methodology, risk assessment, internal controls, and financial reporting frameworks (GAAP,……
5d
ASGN Incorporated
3.5
Non-Profit Audit Senior
Dallas, TX
$83K - $120K (Glassdoor est.)
Easy Apply
Lead audit engagements for non-profit organizations, ensuring compliance with federal and state regulations. Bachelor's degree in Accounting or related field.…
5d
ASGN Incorporated
3.5
Audit Senior
Cranford, NJ
$100K (Employer provided)
Easy Apply
Reviewing audit reports, findings, and recommendations. EBP is a STRONG plus. Our Bonus structure is based on hours billed plus base salary and there are……
5d
Crowe LLP
3.7
Senior Audit Associate - Banking
Livingston, NJ
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
Crowe LLP
3.7
Audit Senior Associate - Commercial Services
Boston, MA
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
ASGN Incorporated
3.5
Audit Senior
Wilmington, DE
$80K - $100K (Employer provided)
Easy Apply
CPA license completed or actively tracking toward licensure. Perform risk assessments and develop detailed audit programs tailored to client risks.…
5d
Crowe LLP
3.7
Audit Senior Associate - Commercial Services
New York, NY
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
Crowe LLP
3.7
Audit Senior Associate - Benefit Plan Services
Livingston, NJ
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
ASGN Incorporated
3.5
Audit Senior
Glastonbury, CT
$85K - $110K (Employer provided)
Easy Apply
Everforth CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law,……
5d
Crowe LLP
3.7
Audit Senior Associate - Financial Services
Cleveland, OH
$71K - $140K (Employer provided)
Easy Apply
Having a CPA license in that state already is even better. This position requires meeting the education requirement for CPA certification in your aligned home……
30d+
Crowe LLP
3.7
Audit Senior Associate - Asset Managment
New York, NY
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
Crowe LLP
3.7
Audit Senior Associate - Public Sector
Livingston, NJ
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+
Crowe LLP
3.7
Audit Senior Associate - Broker Dealer
Livingston, NJ
$71K - $140K (Employer provided)
Easy Apply
This position requires meeting the education requirement for CPA certification in your aligned home office state.…
30d+

Ultragenyx

3.4

Manufacturing Associate II - Upstream - Day Shift (Pitman schedule)

Bedford, MA

$78K - $97K (Employer provided)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Why Join Us?

Be a hero for our rare disease patients

At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won't go – challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life-changing treatments. We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in ways that are most meaningful for them.

Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth – so employees can thrive in all areas of their lives, in and outside of work. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work.

If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team.

Position Summary:

ultrafocused – Work together to fearlessly uncover new possibilities

The Manufacturing Associate II will be a suite-based position within the Gene Therapy Manufacturing facility. The position is a suite/clean room-based position where the Associate II position will be an on the floor technician assigned to the Upstream Manufacturing area.

Expertise will include all cell thaw and culture activities through the various scale of bioreactors up to 2000L and harvest operations.

The position is scheduled from 7am to 7pm on a Pitman rotation.

Work Model:

Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site.

Responsibilities:

Ongoing maintenance of own training file ensuring full training has taken place for all aspects of the production activities in the GTMF area.

Overseeing and driving their training in the GTMF area to enable them to carry out their duties efficiently and compliantly.

Be able to operate efficiently the Veeva Vault system for all quality documentation.

Ensure that high standards of cGMP are adhered to at all times.

Revise GMP documents and templates including batch records, SOPs, OJTs and logbooks.

Ensure that high standards of cGMP documentation completion are adhered to at all times and documentation is left in a reviewable condition at all times.

Demonstrate ownership of the process to ensure that all resources (materials, personnel, documentation etc.) required for processing are available.

Demonstrate a thorough and complete understanding of safety requirements, GMP compliance of the plant and process.

Strive to become a subject matter expert for all "assigned" equipment in the area of control.

Identification of immediate actions/escalation needed to mitigate risk to product, employee safety, or schedule as appropriate.

Identify any Continuous Improvements to the process/equipment and drive through to completion any projects to which may be assigned.

Ensure high standards of housekeeping are adhered to at all times.

Participate in internal/regulatory audits as required.

Attend projects and other meetings as required.

Ensure effective liaison and communication with other departments, maintaining good relations at all times.

Ensure that the appropriate safety policies and systems are adhered to in the GTMF suite.

Ensure that objectives given are met in the appropriate agreed timescale.

Requirements:

High school degree to BS in Engineering, Scientific Discipline or Business or equivalent in experience.

2+ years' experience preferably in pharmaceutical manufacturing or other regulated industry coop, and internship experience is considered.

Experience with viral vectors and/or biological processes.

Strong collaboration, teamwork skills, and communication skills.

Ability and desire to work in a fast-paced, start-up environment is essential.

Independently motivated and detail-oriented with good problem-solving ability.

Need to be able to read, write and understand English, and be proficient in Microsoft (Excel, Word, Outlook).

Physical Demand Requirements

General Manufacturing: Drug Substance/Central Svcs:

Stand for extended periods of time with periodic stooping / bending / kneeling

Able to lift, push, pull up to 50lbs.

Climb ladders and stairs of various heights.

Work in a controlled environment requiring GxP gowning and wear protective clothing over the head, face, hands, feet, and body. This requires the ability to change clothes into appropriate gowning and personal protective equipment.

Certain tasks may require the use of a respirator; medical clearance will be required in advance.

Must remove all make-up, jewelry, and contact lenses while in the manufacturing environment.

Working in temperature-controlled environments (cold rooms).

Full Time employees across the globe enjoy a range of benefits, including, but not limited to:

Generous vacation time and public holidays observed by the company

Volunteer days

Long term incentive and Employee stock purchase plans or equivalent offerings

Employee wellbeing benefits

Fitness reimbursement

Tuition sponsoring

Professional development plans

Benefits vary by region and country

Ultragenyx Pharmaceutical is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at talentacquisition@ultragenyx.com.

See our CCPA Employee and Applicant Privacy Notice.

See our Privacy Policy.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Note to External Recruiters: All candidate activity and open positions are managed strictly through our Human Resources Department. Our Human Resources Department kindly requests that recruiters not contact employees/hiring managers directly in an attempt to solicit business and present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organization. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation. Inquiries on developing a recruiting relationship with us, may be directed to: talentacquisition@ultragenyx.com.

See company reviews

Base pay range

The minimum salary is $78K and the max salary is $97K.

$78K – $97K/yr (Employer provided)

$88K

/yr Median

Bedford, MA

If an employer includes a salary or salary range on their job, we display it as "Employer Provided". If a job has no salary data, Glassdoor displays a "Glassdoor Estimate" if available. To learn more about "Glassdoor Estimates," see our FAQ page.

Working here doesn’t have to be a secret

3.4

Recommend to a friend
Approve of CEO
CEO: Emil Kakkis
154 Ratings

Ultragenyx

3.4

Manufacturing Associate II - Upstream - Day Shift (Pitman schedule)

Bedford, MA

$78K - $97K (Employer provided)

Ultragenyx

3.4

Manufacturing Associate II - Upstream - Day Shift (Pitman schedule)

Bedford, MA

$78K - $97K (Employer provided)

Is your resume a good match?

Use AI to find out how well the skills on your resume fit this job description.

Why Join Us?

Be a hero for our rare disease patients

If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team.

Position Summary:

ultrafocused – Work together to fearlessly uncover new possibilities

Expertise will include all cell thaw and culture activities through the various scale of bioreactors up to 2000L and harvest operations.

The position is scheduled from 7am to 7pm on a Pitman rotation.

Work Model:

Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site.

Responsibilities:

Ongoing maintenance of own training file ensuring full training has taken place for all aspects of the production activities in the GTMF area.

Overseeing and driving their training in the GTMF area to enable them to carry out their duties efficiently and compliantly.

Be able to operate efficiently the Veeva Vault system for all quality documentation.

Ensure that high standards of cGMP are adhered to at all times.

Revise GMP documents and templates including batch records, SOPs, OJTs and logbooks.

Ensure that high standards of cGMP documentation completion are adhered to at all times and documentation is left in a reviewable condition at all times.

Demonstrate ownership of the process to ensure that all resources (materials, personnel, documentation etc.) required for processing are available.

Demonstrate a thorough and complete understanding of safety requirements, GMP compliance of the plant and process.

Strive to become a subject matter expert for all "assigned" equipment in the area of control.

Identification of immediate actions/escalation needed to mitigate risk to product, employee safety, or schedule as appropriate.

Identify any Continuous Improvements to the process/equipment and drive through to completion any projects to which may be assigned.

Ensure high standards of housekeeping are adhered to at all times.

Participate in internal/regulatory audits as required.

Attend projects and other meetings as required.

Ensure effective liaison and communication with other departments, maintaining good relations at all times.

Ensure that the appropriate safety policies and systems are adhered to in the GTMF suite.

Ensure that objectives given are met in the appropriate agreed timescale.

Requirements:

High school degree to BS in Engineering, Scientific Discipline or Business or equivalent in experience.

2+ years' experience preferably in pharmaceutical manufacturing or other regulated industry coop, and internship experience is considered.

Experience with viral vectors and/or biological processes.

Strong collaboration, teamwork skills, and communication skills.

Ability and desire to work in a fast-paced, start-up environment is essential.

Independently motivated and detail-oriented with good problem-solving ability.

Need to be able to read, write and understand English, and be proficient in Microsoft (Excel, Word, Outlook).

Physical Demand Requirements

General Manufacturing: Drug Substance/Central Svcs:

Stand for extended periods of time with periodic stooping / bending / kneeling

Able to lift, push, pull up to 50lbs.

Climb ladders and stairs of various heights.

Work in a controlled environment requiring GxP gowning and wear protective clothing over the head, face, hands, feet, and body. This requires the ability to change clothes into appropriate gowning and personal protective equipment.

Certain tasks may require the use of a respirator; medical clearance will be required in advance.

Must remove all make-up, jewelry, and contact lenses while in the manufacturing environment.

Working in temperature-controlled environments (cold rooms).

Full Time employees across the globe enjoy a range of benefits, including, but not limited to:

Generous vacation time and public holidays observed by the company

Volunteer days

Long term incentive and Employee stock purchase plans or equivalent offerings

Employee wellbeing benefits

Fitness reimbursement

Tuition sponsoring

Professional development plans

Benefits vary by region and country

See our CCPA Employee and Applicant Privacy Notice.

See our Privacy Policy.

See company reviews

Base pay range

The minimum salary is $78K and the max salary is $97K.

$78K – $97K/yr (Employer provided)

$88K

/yr Median

Bedford, MA

Working here doesn’t have to be a secret

3.4

Recommend to a friend
Approve of CEO
CEO: Emil Kakkis
154 Ratings

Are you open to new opportunities?

26,679 Senior Associate - Audit jobs in United States

Position Summary:

Work Model:

Responsibilities:

Requirements:

Base pay range

Working here doesn’t have to be a secret

Position Summary:

Work Model:

Responsibilities:

Requirements:

Base pay range

Working here doesn’t have to be a secret